Item | Value |
---|---|
geneid | 85477 |
ensemblid | ENSG00000006747.15 |
hgncid | 21695 |
symbol | SCIN |
name | scinderin |
refseq_nuc | NM_001112706.3 |
refseq_prot | NP_001106177.1 |
ensembl_nuc | ENST00000297029.10 |
ensembl_prot | ENSP00000297029.5 |
mane_status | MANE Select |
chr | chr7 |
start | 12570720 |
end | 12660182 |
strand | + |
ver | v1.2 |
region | chr7:12570720-12660182 |
region5000 | chr7:12565720-12665182 |
regionname0 | SCIN_chr7_12570720_12660182 |
regionname5000 | SCIN_chr7_12565720_12665182 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 715 | 189 | 26 | 33 | 95 | 10 | 23 | 69 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0002 | 0/0 | 715 | 128 | 40 | 26 | 42 | 5 | 15 | 27 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0003 | 0/0 | 715 | 10 | 0 | 7 | 3 | 0 | 0 | 3 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0004 | 0/0 | 715 | 7 | 3 | 3 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0005 | 0/0 | 715 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0006 | 0/0 | 715 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0007 | 0/0 | 55 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(50): Show |
chr7 | 12565720 | 12665182 |
a0008 | 0/0 | 715 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0009 | 0/0 | 715 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0010 | 0/0 | 715 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0011 | 0/0 | 715 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0012 | 0/0 | 715 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0013 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0014 | 0/0 | 71 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MPTWC others(66): Show |
chr7 | 12565720 | 12665182 |
a0015 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0016 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0017 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0018 | 0/0 | 715 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
a0019 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | MAREL others(710): Show |
chr7 | 12565720 | 12665182 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2145 | 189 | 26 | 33 | 95 | 10 | 23 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0002c0002 | 0/0 | 2145 | 82 | 11 | 20 | 35 | 4 | 12 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0002c0003 | 0/0 | 2145 | 40 | 27 | 3 | 7 | 1 | 2 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0002c0010 | 0/0 | 2145 | 3 | 0 | 2 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0002c0014 | 0/0 | 2145 | 2 | 2 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0002c0019 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0003c0004 | 0/0 | 2145 | 10 | 0 | 7 | 3 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0004c0005 | 0/0 | 2145 | 7 | 3 | 3 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0005c0007 | 0/0 | 2145 | 6 | 6 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0006c0006 | 0/0 | 2145 | 6 | 0 | 0 | 6 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0007c0008 | 0/0 | 2145 | 5 | 0 | 0 | 5 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0007c0023 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0008c0009 | 0/0 | 2145 | 4 | 4 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0009c0012 | 0/0 | 2145 | 3 | 3 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0010c0011 | 0/0 | 2145 | 3 | 3 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0011c0013 | 0/0 | 2145 | 2 | 1 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0012c0018 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0013c0020 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0014c0024 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATTGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0015c0021 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0016c0016 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0017c0022 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0018c0017 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 | ||
a0019c0015 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | ATGGC others(2140): Show |
chr7 | 12565720 | 12665182 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 9682 | 19 | 0 | 3 | 13 | 0 | 2 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0002 | 0/0 | 9682 | 7 | 0 | 2 | 2 | 1 | 2 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0003 | 0/0 | 9685 | 16 | 0 | 3 | 10 | 2 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0004 | 0/0 | 9685 | 3 | 0 | 3 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0005 | 0/0 | 9682 | 8 | 0 | 1 | 3 | 3 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0006 | 0/0 | 9673 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9668): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0007 | 0/0 | 9682 | 3 | 0 | 0 | 3 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0008 | 0/0 | 9682 | 2 | 0 | 0 | 1 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0009 | 0/0 | 9683 | 5 | 0 | 0 | 5 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0010 | 0/0 | 9682 | 3 | 0 | 0 | 1 | 0 | 2 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0011 | 0/0 | 9682 | 4 | 0 | 0 | 4 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0012 | 0/0 | 9681 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0013 | 0/0 | 9680 | 2 | 0 | 1 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0014 | 0/0 | 9684 | 2 | 2 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0016 | 0/0 | 9679 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9674): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0017 | 0/0 | 9683 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0018 | 0/0 | 9682 | 2 | 0 | 0 | 2 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0019 | 0/0 | 9680 | 3 | 0 | 2 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0020 | 0/0 | 9681 | 2 | 2 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0021 | 0/0 | 9684 | 2 | 0 | 0 | 2 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0022 | 0/0 | 9685 | 2 | 0 | 0 | 0 | 0 | 2 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0023 | 0/0 | 9683 | 2 | 0 | 0 | 1 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0024 | 0/0 | 9692 | 3 | 0 | 0 | 3 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9687): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0025 | 0/0 | 9681 | 2 | 0 | 0 | 2 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0027 | 0/0 | 9697 | 2 | 0 | 2 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9692): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0028 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0029 | 0/0 | 9681 | 2 | 0 | 0 | 0 | 0 | 2 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0030 | 0/0 | 9682 | 2 | 0 | 2 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0032 | 0/0 | 9683 | 2 | 0 | 0 | 1 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0033 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0035 | 0/0 | 9690 | 2 | 0 | 0 | 2 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9685): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0037 | 0/0 | 9683 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0040 | 0/0 | 9680 | 2 | 0 | 2 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0042 | 0/0 | 9660 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9655): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0043 | 0/0 | 9682 | 2 | 2 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0044 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0045 | 0/0 | 9683 | 2 | 0 | 0 | 2 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0050 | 0/0 | 9673 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9668): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0051 | 0/0 | 9680 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0052 | 0/0 | 9681 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0053 | 0/0 | 9682 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0054 | 0/0 | 9699 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9694): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0055 | 0/0 | 9689 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9684): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0066 | 0/0 | 9686 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9681): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0067 | 0/0 | 9685 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0070 | 0/0 | 9684 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0071 | 0/0 | 9685 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0072 | 0/1 | 9669 | 1 | 0 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9664): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0073 | 0/0 | 9685 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0074 | 0/0 | 9684 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0075 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0076 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0083 | 0/0 | 9684 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0086 | 0/0 | 9682 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0087 | 0/0 | 9683 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0090 | 0/0 | 9682 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0092 | 0/0 | 9682 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0093 | 0/0 | 9684 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0094 | 0/0 | 9684 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0095 | 0/0 | 9685 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0096 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0097 | 0/0 | 9684 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0099 | 0/0 | 9688 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9683): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0100 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0101 | 0/0 | 9681 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0102 | 0/0 | 9689 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9684): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0103 | 0/0 | 9685 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0105 | 0/0 | 9681 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0107 | 0/0 | 9667 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9662): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0108 | 0/0 | 9680 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0109 | 0/0 | 9683 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0112 | 0/0 | 9679 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9674): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0115 | 0/0 | 9681 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0116 | 0/0 | 9696 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9691): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0117 | 0/0 | 9694 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9689): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0118 | 0/0 | 9686 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9681): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0119 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0120 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0121 | 0/0 | 9682 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0122 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0123 | 0/0 | 9680 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0124 | 0/0 | 9682 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0125 | 0/0 | 9695 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9690): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0127 | 0/0 | 9684 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0131 | 0/0 | 9686 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9681): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0132 | 0/0 | 9683 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0133 | 0/0 | 9683 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0136 | 0/0 | 9672 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9667): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0137 | 0/0 | 9694 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9689): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0138 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0141 | 0/0 | 9680 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0145 | 0/0 | 9665 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9660): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0149 | 0/0 | 9685 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0151 | 0/0 | 9694 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9689): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0152 | 0/0 | 9690 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9685): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0153 | 0/0 | 9688 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9683): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0154 | 0/0 | 9681 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0162 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0163 | 0/0 | 9684 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0164 | 0/0 | 9682 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0166 | 0/0 | 9683 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0170 | 0/0 | 9685 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0172 | 0/0 | 9684 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0173 | 0/0 | 9684 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0176 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0179 | 0/0 | 9682 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0181 | 0/0 | 9680 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0183 | 0/0 | 9681 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0001c0001t0185 | 0/0 | 9686 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9681): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0001 | 0/0 | 9682 | 9 | 0 | 2 | 5 | 1 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0002 | 0/0 | 9682 | 11 | 2 | 2 | 2 | 0 | 5 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0003 | 0/0 | 9685 | 2 | 0 | 2 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0004 | 0/0 | 9685 | 2 | 0 | 1 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0005 | 0/0 | 9682 | 4 | 1 | 2 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0007 | 0/0 | 9682 | 3 | 0 | 0 | 3 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0008 | 0/0 | 9682 | 2 | 0 | 1 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0010 | 0/0 | 9682 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0012 | 0/0 | 9681 | 4 | 1 | 0 | 3 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0013 | 0/0 | 9680 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0015 | 0/0 | 9683 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0016 | 0/0 | 9679 | 2 | 0 | 0 | 2 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9674): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0018 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0020 | 0/0 | 9681 | 2 | 2 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0021 | 0/0 | 9684 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0023 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0026 | 0/0 | 9682 | 2 | 0 | 1 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0031 | 0/0 | 9679 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9674): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0033 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0038 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0041 | 0/0 | 9682 | 2 | 0 | 2 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0065 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0069 | 0/0 | 9680 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0077 | 0/0 | 9684 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0078 | 0/0 | 9684 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0079 | 0/0 | 9679 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9674): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0084 | 0/0 | 9681 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0091 | 0/0 | 9693 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9688): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0098 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0113 | 0/0 | 9679 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9674): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0114 | 0/0 | 9680 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0126 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0129 | 0/0 | 9682 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0130 | 0/0 | 9683 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0140 | 0/0 | 9684 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0150 | 0/0 | 9681 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0155 | 0/0 | 9685 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0156 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0157 | 0/0 | 9681 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0158 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0167 | 0/0 | 9681 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0168 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0169 | 0/0 | 9682 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0174 | 0/0 | 9682 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0175 | 0/0 | 9681 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0177 | 0/0 | 9680 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0178 | 0/0 | 9678 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9673): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0180 | 0/0 | 9684 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0002c0002t0182 | 0/0 | 9683 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0002 | 0/0 | 9682 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0006 | 0/0 | 9673 | 4 | 4 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9668): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0008 | 0/0 | 9682 | 2 | 0 | 2 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0010 | 0/0 | 9682 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0013 | 0/0 | 9680 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0014 | 0/0 | 9684 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0015 | 0/0 | 9683 | 3 | 3 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0016 | 0/0 | 9679 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9674): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0017 | 0/0 | 9683 | 3 | 3 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0022 | 0/0 | 9685 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0036 | 0/0 | 9682 | 2 | 2 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0037 | 0/0 | 9683 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0046 | 0/0 | 9695 | 2 | 2 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9690): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0047 | 0/0 | 9689 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9684): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0056 | 0/0 | 9685 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0057 | 0/0 | 9685 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0058 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0059 | 0/0 | 9681 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0060 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0061 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0062 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0063 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0089 | 0/0 | 9685 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0134 | 0/0 | 9679 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9674): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0142 | 0/0 | 9676 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9671): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0143 | 0/0 | 9683 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0144 | 0/0 | 9685 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0146 | 0/0 | 9667 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9662): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0161 | 0/0 | 9684 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0002c0003t0165 | 0/0 | 9684 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0002c0010t0001 | 0/0 | 9682 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0010t0068 | 0/0 | 9682 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0010t0128 | 0/0 | 9682 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0002c0014t0006 | 0/0 | 9673 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9668): Show |
chr7 | 12565720 | 12665182 |
a0002c0014t0184 | 0/0 | 9683 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0002c0019t0064 | 0/0 | 9679 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9674): Show |
chr7 | 12565720 | 12665182 |
a0003c0004t0002 | 0/0 | 9682 | 3 | 0 | 3 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0003c0004t0004 | 0/0 | 9685 | 6 | 0 | 3 | 3 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0003c0004t0007 | 0/0 | 9682 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0004c0005t0006 | 0/0 | 9673 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9668): Show |
chr7 | 12565720 | 12665182 |
a0004c0005t0014 | 0/0 | 9684 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0004c0005t0019 | 0/0 | 9680 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0004c0005t0042 | 0/0 | 9660 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9655): Show |
chr7 | 12565720 | 12665182 |
a0004c0005t0049 | 0/0 | 9680 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0004c0005t0104 | 0/0 | 9681 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9676): Show |
chr7 | 12565720 | 12665182 |
a0004c0005t0106 | 0/0 | 9685 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0005c0007t0006 | 0/0 | 9673 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9668): Show |
chr7 | 12565720 | 12665182 |
a0005c0007t0034 | 0/0 | 9678 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9673): Show |
chr7 | 12565720 | 12665182 |
a0005c0007t0047 | 0/0 | 9689 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9684): Show |
chr7 | 12565720 | 12665182 |
a0005c0007t0048 | 0/0 | 9685 | 2 | 2 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0005c0007t0081 | 0/0 | 9679 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9674): Show |
chr7 | 12565720 | 12665182 |
a0006c0006t0007 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0006c0006t0011 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0006c0006t0018 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0006c0006t0028 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0006c0006t0139 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0006c0006t0171 | 0/0 | 9684 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0007c0008t0003 | 0/0 | 9685 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0007c0008t0009 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0007c0008t0039 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0007c0008t0088 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0007c0008t0147 | 0/0 | 9682 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0007c0023t0039 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0008c0009t0006 | 0/0 | 9673 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9668): Show |
chr7 | 12565720 | 12665182 |
a0008c0009t0110 | 0/0 | 9670 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9665): Show |
chr7 | 12565720 | 12665182 |
a0008c0009t0159 | 0/0 | 9682 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0008c0009t0160 | 0/0 | 9677 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9672): Show |
chr7 | 12565720 | 12665182 |
a0009c0012t0080 | 0/0 | 9680 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
a0009c0012t0082 | 0/0 | 9678 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9673): Show |
chr7 | 12565720 | 12665182 |
a0009c0012t0085 | 0/0 | 9682 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0010c0011t0031 | 0/0 | 9679 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9674): Show |
chr7 | 12565720 | 12665182 |
a0010c0011t0111 | 0/0 | 9678 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9673): Show |
chr7 | 12565720 | 12665182 |
a0010c0011t0135 | 0/0 | 9679 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9674): Show |
chr7 | 12565720 | 12665182 |
a0011c0013t0009 | 0/0 | 9683 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0011c0013t0014 | 0/0 | 9684 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9679): Show |
chr7 | 12565720 | 12665182 |
a0012c0018t0002 | 0/0 | 9682 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0013c0020t0038 | 0/0 | 9683 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0014c0024t0044 | 0/0 | 9683 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9678): Show |
chr7 | 12565720 | 12665182 |
a0015c0021t0004 | 0/0 | 9685 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9680): Show |
chr7 | 12565720 | 12665182 |
a0016c0016t0148 | 0/0 | 9658 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9653): Show |
chr7 | 12565720 | 12665182 |
a0017c0022t0034 | 0/0 | 9678 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9673): Show |
chr7 | 12565720 | 12665182 |
a0018c0017t0008 | 0/0 | 9682 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9677): Show |
chr7 | 12565720 | 12665182 |
a0019c0015t0013 | 0/0 | 9680 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | TGCTG others(9675): Show |
chr7 | 12565720 | 12665182 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0120 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0008g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0008g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0009g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0009g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0009g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0009g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0010g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0010g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0010g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0011g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0011g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0011g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0012g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0013g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0013g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0014g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0014g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0016g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0017g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0018g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0018g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0019g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0019g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0019g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0020g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0020g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0021g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0021g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0022g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0022g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0023g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0023g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0024g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0024g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0024g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0025g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0025g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0027g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0027g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0028g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0029g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0029g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0030g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0030g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0032g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0032g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0033g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0035g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0035g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0037g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0040g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0040g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0042g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0043g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0043g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0044g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0045g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0045g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0050g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0051g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0052g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0053g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0054g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0055g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0066g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0067g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0070g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0071g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0072g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0073g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0074g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0075g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0076g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0083g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0086g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0087g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0090g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0092g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0093g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0094g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0095g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0096g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0097g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0099g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0100g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0101g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0102g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0103g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0105g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0107g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0108g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0109g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0112g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0115g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0116g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0117g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0118g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0119g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0120g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0121g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0122g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0123g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0124g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0125g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0127g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0131g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0132g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0133g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0136g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0137g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0138g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0141g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0145g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0149g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0151g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0152g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0153g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0154g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0162g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0163g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0164g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0166g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0170g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0172g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0173g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0176g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0179g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0181g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0183g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0001c0001t0185g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0005g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0007g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0007g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0007g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0008g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0008g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0010g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0012g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0012g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0012g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0012g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0013g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0015g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0016g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0016g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0018g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0020g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0020g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0021g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0023g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0026g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0026g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0031g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0033g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0038g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0041g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0041g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0065g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0069g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0077g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0078g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0079g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0084g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0091g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0098g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0113g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0114g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0126g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0129g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0130g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0140g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0150g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0155g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0156g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0157g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0158g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0167g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0168g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0169g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0174g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0175g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0177g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0178g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0180g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0002t0182g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0006g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0008g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0008g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0010g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0013g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0014g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0015g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0015g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0015g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0016g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0017g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0017g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0022g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0036g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0037g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0046g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0046g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0047g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0056g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0057g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0058g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0059g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0060g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0061g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0062g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0063g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0089g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0134g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0142g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0143g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0144g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0146g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0161g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0003t0165g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0010t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0010t0068g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0010t0128g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0014t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0014t0184g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0002c0019t0064g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0003c0004t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0003c0004t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0003c0004t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0003c0004t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0003c0004t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0003c0004t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0003c0004t0007g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0004c0005t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0004c0005t0014g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0004c0005t0019g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0004c0005t0042g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0004c0005t0049g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0004c0005t0104g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0004c0005t0106g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0005c0007t0006g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0005c0007t0034g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0005c0007t0047g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0005c0007t0048g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0005c0007t0081g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0006c0006t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0006c0006t0011g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0006c0006t0018g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0006c0006t0028g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0006c0006t0139g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0006c0006t0171g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0007c0008t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0007c0008t0009g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0007c0008t0039g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0007c0008t0088g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0007c0008t0147g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0007c0023t0039g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0008c0009t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0008c0009t0110g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0008c0009t0159g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0008c0009t0160g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0009c0012t0080g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0009c0012t0082g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0009c0012t0085g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0010c0011t0031g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0010c0011t0111g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0010c0011t0135g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0011c0013t0009g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0011c0013t0014g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0012c0018t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0013c0020t0038g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0014c0024t0044g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0015c0021t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0016c0016t0148g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0017c0022t0034g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0018c0017t0008g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
a0019c0015t0013g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0179 | g0014 | EUR | GBR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00099 | hp2 | a0002 | c0003 | t0013 | g0256 | EUR | GBR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00140 | hp1 | a0012 | c0018 | t0002 | g0302 | EUR | GBR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00140 | hp2 | a0001 | c0001 | t0032 | g0082 | EUR | GBR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0311 | EUR | FIN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00323 | hp2 | a0001 | c0001 | t0019 | g0166 | EUR | FIN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00408 | hp1 | a0001 | c0001 | t0045 | g0053 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00423 | hp1 | a0001 | c0001 | t0094 | g0102 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00423 | hp2 | a0002 | c0002 | t0007 | g0275 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00438 | hp1 | a0001 | c0001 | t0173 | g0081 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00544 | hp1 | a0001 | c0001 | t0131 | g0173 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00544 | hp2 | a0002 | c0002 | t0069 | g0269 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00558 | hp1 | a0001 | c0001 | t0007 | g0086 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00558 | hp2 | a0002 | c0002 | t0098 | g0253 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00597 | hp2 | a0002 | c0003 | t0058 | g0361 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00621 | hp2 | a0002 | c0002 | t0005 | g0262 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00642 | hp1 | a0002 | c0002 | t0041 | g0326 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00642 | hp2 | a0002 | c0002 | t0174 | g0324 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00673 | hp1 | a0002 | c0002 | t0158 | g0298 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00673 | hp2 | a0001 | c0001 | t0100 | g0222 | EAS | CHS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00735 | hp1 | a0003 | c0004 | t0002 | g0003 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00738 | hp1 | a0004 | c0005 | t0019 | g0177 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00738 | hp2 | a0001 | c0001 | t0054 | g0345 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00741 | hp1 | a0001 | c0001 | t0055 | g0348 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG00741 | hp2 | a0004 | c0005 | t0042 | g0116 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01069 | hp1 | a0003 | c0004 | t0004 | g0148 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01070 | hp1 | a0003 | c0004 | t0002 | g0149 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01070 | hp2 | a0001 | c0001 | t0040 | g0225 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01071 | hp1 | a0003 | c0004 | t0002 | g0003 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01081 | hp1 | a0001 | c0001 | t0040 | g0226 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01081 | hp2 | a0001 | c0001 | t0132 | g0186 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0267 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01106 | hp2 | a0002 | c0010 | t0068 | g0265 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0268 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01109 | hp2 | a0001 | c0001 | t0083 | g0118 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01167 | hp1 | a0001 | c0001 | t0027 | g0013 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01167 | hp2 | a0001 | c0001 | t0105 | g0040 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01168 | hp1 | a0002 | c0002 | t0182 | g0333 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01168 | hp2 | a0001 | c0001 | t0030 | g0115 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01169 | hp1 | a0001 | c0001 | t0030 | g0194 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01169 | hp2 | a0001 | c0001 | t0027 | g0042 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01175 | hp1 | a0001 | c0001 | t0051 | g0347 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01175 | hp2 | a0001 | c0001 | t0019 | g0230 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01192 | hp1 | a0003 | c0004 | t0004 | g0134 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01192 | hp2 | a0002 | c0002 | t0005 | g0319 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01243 | hp1 | a0002 | c0002 | t0031 | g0285 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01243 | hp2 | a0002 | c0002 | t0041 | g0325 | AMR | PUR | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01255 | hp1 | a0001 | c0001 | t0019 | g0224 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01255 | hp2 | a0002 | c0019 | t0064 | g0354 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01256 | hp1 | a0002 | c0003 | t0008 | g0249 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01256 | hp2 | a0001 | c0001 | t0052 | g0343 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01257 | hp1 | a0002 | c0002 | t0129 | g0007 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01257 | hp2 | a0002 | c0002 | t0114 | g0289 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01258 | hp1 | a0002 | c0002 | t0130 | g0007 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01258 | hp2 | a0001 | c0001 | t0053 | g0344 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01261 | hp1 | a0001 | c0001 | t0013 | g0020 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01261 | hp2 | a0002 | c0003 | t0008 | g0250 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01346 | hp1 | a0002 | c0002 | t0004 | g0290 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01346 | hp2 | a0002 | c0002 | t0003 | g0305 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0213 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01361 | hp2 | a0001 | c0001 | t0154 | g0137 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0252 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01433 | hp2 | a0002 | c0003 | t0010 | g0287 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0322 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01496 | hp2 | a0001 | c0001 | t0153 | g0018 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0139 | EUR | IBS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01515 | hp2 | a0002 | c0002 | t0169 | g0293 | EUR | IBS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0084 | EUR | IBS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0229 | EUR | IBS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0158 | EUR | IBS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0083 | EUR | IBS | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01884 | hp1 | a0001 | c0001 | t0043 | g0227 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01884 | hp2 | a0001 | c0001 | t0070 | g0183 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01891 | hp1 | a0002 | c0003 | t0036 | g0006 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01891 | hp2 | a0001 | c0001 | t0102 | g0188 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01928 | hp1 | a0002 | c0002 | t0005 | g0270 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01928 | hp2 | a0001 | c0001 | t0005 | g0212 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01943 | hp1 | a0002 | c0002 | t0026 | g0291 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01943 | hp2 | a0013 | c0020 | t0038 | g0272 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01952 | hp2 | a0002 | c0010 | t0128 | g0266 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01975 | hp1 | a0011 | c0013 | t0009 | g0257 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01975 | hp2 | a0003 | c0004 | t0007 | g0123 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01978 | hp1 | a0004 | c0005 | t0049 | g0346 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01978 | hp2 | a0002 | c0002 | t0091 | g0292 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01993 | hp2 | a0002 | c0002 | t0008 | g0271 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0108 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02004 | hp2 | a0003 | c0004 | t0004 | g0133 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02015 | hp1 | a0002 | c0002 | t0026 | g0352 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02027 | hp1 | a0002 | c0002 | t0016 | g0274 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02040 | hp2 | a0001 | c0001 | t0024 | g0099 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02055 | hp1 | a0001 | c0001 | t0093 | g0043 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02055 | hp2 | a0002 | c0003 | t0036 | g0006 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0351 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02080 | hp1 | a0002 | c0002 | t0126 | g0315 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02083 | hp1 | a0014 | c0024 | t0044 | g0085 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02129 | hp1 | a0001 | c0001 | t0025 | g0218 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02129 | hp2 | a0001 | c0001 | t0009 | g0209 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02132 | hp1 | a0001 | c0001 | t0066 | g0045 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02135 | hp1 | a0001 | c0001 | t0035 | g0033 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02135 | hp2 | a0001 | c0001 | t0033 | g0127 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02145 | hp1 | a0005 | c0007 | t0081 | g0336 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02145 | hp2 | a0002 | c0002 | t0010 | g0317 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02155 | hp1 | a0001 | c0001 | t0023 | g0162 | EAS | CDX | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02165 | hp1 | a0001 | c0001 | t0018 | g0110 | EAS | CDX | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02257 | hp1 | a0002 | c0003 | t0017 | g0233 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02257 | hp2 | a0009 | c0012 | t0085 | g0282 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02258 | hp1 | a0002 | c0003 | t0161 | g0067 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0320 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02280 | hp1 | a0001 | c0001 | t0141 | g0199 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02280 | hp2 | a0002 | c0002 | t0020 | g0244 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0128 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02293 | hp2 | a0015 | c0021 | t0004 | g0323 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02300 | hp1 | a0001 | c0001 | t0071 | g0022 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02300 | hp2 | a0001 | c0001 | t0086 | g0107 | AMR | PEL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02451 | hp1 | a0002 | c0003 | t0037 | g0071 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02451 | hp2 | a0005 | c0007 | t0047 | g0338 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02523 | hp1 | a0002 | c0003 | t0056 | g0358 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02523 | hp2 | a0002 | c0002 | t0038 | g0264 | EAS | KHV | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02572 | hp1 | a0001 | c0001 | t0185 | g0200 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02572 | hp2 | a0002 | c0002 | t0079 | g0280 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02602 | hp1 | a0001 | c0001 | t0112 | g0178 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02602 | hp2 | a0001 | c0001 | t0092 | g0141 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02622 | hp1 | a0001 | c0001 | t0017 | g0220 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02622 | hp2 | a0002 | c0003 | t0143 | g0232 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02630 | hp1 | a0011 | c0013 | t0014 | g0238 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02630 | hp2 | a0001 | c0001 | t0014 | g0021 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0310 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02717 | hp1 | a0002 | c0003 | t0047 | g0070 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02717 | hp2 | a0002 | c0014 | t0184 | g0059 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02723 | hp1 | a0001 | c0001 | t0014 | g0112 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02723 | hp2 | a0008 | c0009 | t0110 | g0240 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0239 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02735 | hp2 | a0002 | c0002 | t0078 | g0321 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02809 | hp1 | a0008 | c0009 | t0159 | g0241 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02809 | hp2 | a0001 | c0001 | t0037 | g0012 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02886 | hp1 | a0002 | c0002 | t0012 | g0278 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02886 | hp2 | a0016 | c0016 | t0148 | g0168 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02895 | hp1 | a0005 | c0007 | t0048 | g0009 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02895 | hp2 | a0001 | c0001 | t0181 | g0017 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02896 | hp1 | a0001 | c0001 | t0166 | g0011 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02896 | hp2 | a0010 | c0011 | t0031 | g0005 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02897 | hp1 | a0005 | c0007 | t0048 | g0009 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02897 | hp2 | a0010 | c0011 | t0111 | g0005 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02922 | hp1 | a0001 | c0001 | t0020 | g0113 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02922 | hp2 | a0004 | c0005 | t0006 | g0221 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02965 | hp1 | a0001 | c0001 | t0145 | g0041 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02965 | hp2 | a0002 | c0002 | t0180 | g0245 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02970 | hp1 | a0002 | c0014 | t0006 | g0060 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02970 | hp2 | a0008 | c0009 | t0006 | g0242 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02976 | hp1 | a0010 | c0011 | t0135 | g0353 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02976 | hp2 | a0001 | c0001 | t0183 | g0165 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03017 | hp1 | a0001 | c0001 | t0108 | g0204 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03017 | hp2 | a0002 | c0002 | t0157 | g0328 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03041 | hp1 | a0002 | c0002 | t0113 | g0277 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03041 | hp2 | a0002 | c0003 | t0165 | g0068 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03098 | hp1 | a0004 | c0005 | t0014 | g0202 | AFR | MSL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03098 | hp2 | a0001 | c0001 | t0050 | g0349 | AFR | MSL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03130 | hp1 | a0001 | c0001 | t0164 | g0197 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03139 | hp1 | a0002 | c0003 | t0046 | g0061 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03139 | hp2 | a0002 | c0003 | t0017 | g0231 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03195 | hp1 | a0002 | c0003 | t0006 | g0337 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03195 | hp2 | a0017 | c0022 | t0034 | g0281 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03225 | hp1 | a0002 | c0003 | t0014 | g0069 | AFR | MSL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03225 | hp2 | a0002 | c0003 | t0006 | g0236 | AFR | MSL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0144 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03239 | hp2 | a0002 | c0002 | t0167 | g0331 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03453 | hp1 | a0009 | c0012 | t0080 | g0283 | AFR | MSL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03453 | hp2 | a0002 | c0003 | t0017 | g0066 | AFR | MSL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03486 | hp1 | a0008 | c0009 | t0160 | g0243 | AFR | MSL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03486 | hp2 | a0002 | c0003 | t0006 | g0063 | AFR | MSL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03490 | hp1 | a0001 | c0001 | t0022 | g0174 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03490 | hp2 | a0001 | c0001 | t0008 | g0096 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03491 | hp1 | a0002 | c0010 | t0001 | g0261 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0332 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0329 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03492 | hp2 | a0001 | c0001 | t0022 | g0175 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03516 | hp1 | a0001 | c0001 | t0136 | g0117 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0247 | AFR | ESN | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03540 | hp1 | a0002 | c0002 | t0015 | g0279 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03540 | hp2 | a0001 | c0001 | t0043 | g0228 | AFR | GWD | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03579 | hp1 | a0001 | c0001 | t0121 | g0201 | AFR | MSL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03579 | hp2 | a0002 | c0003 | t0142 | g0341 | AFR | MSL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03654 | hp1 | a0001 | c0001 | t0109 | g0160 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03654 | hp2 | a0001 | c0001 | t0010 | g0167 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03669 | hp2 | a0001 | c0001 | t0149 | g0157 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03688 | hp1 | a0002 | c0003 | t0002 | g0255 | SAS | STU | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03688 | hp2 | a0001 | c0001 | t0029 | g0076 | SAS | STU | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03704 | hp1 | a0001 | c0001 | t0023 | g0140 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03704 | hp2 | a0002 | c0002 | t0077 | g0314 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0304 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03710 | hp2 | a0001 | c0001 | t0123 | g0057 | SAS | PJL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03831 | hp2 | a0001 | c0001 | t0163 | g0035 | SAS | BEB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03834 | hp1 | a0002 | c0002 | t0150 | g0318 | SAS | BEB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03834 | hp2 | a0002 | c0002 | t0175 | g0251 | SAS | BEB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03927 | hp2 | a0001 | c0001 | t0010 | g0142 | SAS | BEB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG04115 | hp1 | a0001 | c0001 | t0029 | g0019 | SAS | STU | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG04115 | hp2 | a0004 | c0005 | t0104 | g0138 | SAS | STU | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG04184 | hp1 | a0018 | c0017 | t0008 | g0216 | SAS | BEB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG04184 | hp2 | a0001 | c0001 | t0090 | g0015 | SAS | BEB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | STU | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG04199 | hp2 | a0002 | c0003 | t0022 | g0248 | SAS | STU | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18522 | hp1 | a0001 | c0001 | t0133 | g0198 | AFR | YRI | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18522 | hp2 | a0005 | c0007 | t0034 | g0350 | AFR | YRI | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18747 | hp1 | a0002 | c0002 | t0177 | g0263 | EAS | CHB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18747 | hp2 | a0001 | c0001 | t0025 | g0028 | EAS | CHB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18906 | hp1 | a0001 | c0001 | t0042 | g0195 | AFR | YRI | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18906 | hp2 | a0002 | c0003 | t0015 | g0065 | AFR | YRI | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18939 | hp1 | a0001 | c0001 | t0074 | g0052 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18939 | hp2 | a0002 | c0002 | t0168 | g0316 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18940 | hp1 | a0006 | c0006 | t0171 | g0147 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18940 | hp2 | a0001 | c0001 | t0075 | g0179 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18941 | hp1 | a0001 | c0001 | t0176 | g0171 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18941 | hp2 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18943 | hp2 | a0002 | c0002 | t0007 | g0288 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18944 | hp1 | a0002 | c0002 | t0012 | g0334 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18944 | hp2 | a0002 | c0003 | t0061 | g0359 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18945 | hp1 | a0006 | c0006 | t0018 | g0176 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18945 | hp2 | a0001 | c0001 | t0162 | g0090 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18946 | hp1 | a0002 | c0002 | t0178 | g0299 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18946 | hp2 | a0001 | c0001 | t0152 | g0161 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18947 | hp1 | a0002 | c0002 | t0012 | g0286 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18947 | hp2 | a0001 | c0001 | t0122 | g0210 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18949 | hp1 | a0002 | c0002 | t0018 | g0296 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18949 | hp2 | a0001 | c0001 | t0021 | g0010 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18951 | hp1 | a0001 | c0001 | t0024 | g0131 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18951 | hp2 | a0007 | c0008 | t0009 | g0172 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18952 | hp2 | a0002 | c0002 | t0007 | g0008 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18954 | hp2 | a0002 | c0003 | t0060 | g0356 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18956 | hp1 | a0002 | c0002 | t0033 | g0008 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18956 | hp2 | a0001 | c0001 | t0097 | g0189 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18959 | hp1 | a0002 | c0002 | t0023 | g0254 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18959 | hp2 | a0001 | c0001 | t0115 | g0100 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18960 | hp1 | a0001 | c0001 | t0021 | g0207 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18960 | hp2 | a0001 | c0001 | t0012 | g0106 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18964 | hp1 | a0001 | c0001 | t0011 | g0190 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18964 | hp2 | a0001 | c0001 | t0011 | g0034 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18965 | hp1 | a0003 | c0004 | t0004 | g0001 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18965 | hp2 | a0002 | c0002 | t0140 | g0300 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18966 | hp1 | a0002 | c0002 | t0156 | g0306 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18966 | hp2 | a0007 | c0008 | t0147 | g0156 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18968 | hp1 | a0001 | c0001 | t0099 | g0103 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18968 | hp2 | a0001 | c0001 | t0118 | g0049 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18970 | hp1 | a0001 | c0001 | t0116 | g0136 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18970 | hp2 | a0001 | c0001 | t0073 | g0036 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0164 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18971 | hp2 | a0019 | c0015 | t0013 | g0038 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18975 | hp1 | a0001 | c0001 | t0007 | g0051 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18975 | hp2 | a0001 | c0001 | t0008 | g0215 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18977 | hp1 | a0007 | c0008 | t0039 | g0155 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18978 | hp1 | a0001 | c0001 | t0127 | g0044 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18978 | hp2 | a0002 | c0002 | t0065 | g0297 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18979 | hp1 | a0002 | c0002 | t0004 | g0273 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18979 | hp2 | a0001 | c0001 | t0045 | g0211 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18980 | hp1 | a0001 | c0001 | t0101 | g0122 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18980 | hp2 | a0001 | c0001 | t0009 | g0180 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18981 | hp1 | a0001 | c0001 | t0009 | g0025 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18981 | hp2 | a0001 | c0001 | t0137 | g0114 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18982 | hp2 | a0003 | c0004 | t0004 | g0001 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18983 | hp1 | a0001 | c0001 | t0151 | g0109 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18983 | hp2 | a0001 | c0001 | t0009 | g0031 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18987 | hp2 | a0002 | c0002 | t0021 | g0295 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18991 | hp1 | a0001 | c0001 | t0032 | g0105 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18991 | hp2 | a0007 | c0023 | t0039 | g0135 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18992 | hp2 | a0002 | c0002 | t0016 | g0312 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18993 | hp1 | a0006 | c0006 | t0011 | g0152 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA18993 | hp2 | a0001 | c0001 | t0125 | g0111 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19000 | hp2 | a0001 | c0001 | t0095 | g0039 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19002 | hp2 | a0002 | c0002 | t0155 | g0307 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19004 | hp1 | a0007 | c0008 | t0003 | g0154 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0208 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19007 | hp1 | a0001 | c0001 | t0011 | g0046 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19007 | hp2 | a0007 | c0008 | t0088 | g0077 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19009 | hp1 | a0002 | c0002 | t0012 | g0303 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19009 | hp2 | a0002 | c0003 | t0063 | g0357 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19010 | hp2 | a0001 | c0001 | t0120 | g0075 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19011 | hp2 | a0001 | c0001 | t0138 | g0080 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0301 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19030 | hp1 | a0002 | c0003 | t0146 | g0062 | AFR | LWK | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19030 | hp2 | a0002 | c0003 | t0089 | g0235 | AFR | LWK | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19043 | hp1 | a0002 | c0003 | t0015 | g0340 | AFR | LWK | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19043 | hp2 | a0001 | c0001 | t0020 | g0196 | AFR | LWK | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19057 | hp1 | a0001 | c0001 | t0016 | g0023 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19057 | hp2 | a0003 | c0004 | t0004 | g0001 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19062 | hp1 | a0001 | c0001 | t0170 | g0074 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19062 | hp2 | a0001 | c0001 | t0096 | g0050 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19064 | hp1 | a0001 | c0001 | t0117 | g0030 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19064 | hp2 | a0001 | c0001 | t0107 | g0097 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19065 | hp2 | a0001 | c0001 | t0067 | g0205 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19066 | hp2 | a0006 | c0006 | t0028 | g0129 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19068 | hp1 | a0001 | c0001 | t0035 | g0104 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19068 | hp2 | a0001 | c0001 | t0044 | g0130 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19074 | hp1 | a0002 | c0003 | t0062 | g0355 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19079 | hp1 | a0001 | c0001 | t0172 | g0024 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19079 | hp2 | a0001 | c0001 | t0010 | g0150 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19080 | hp1 | a0001 | c0001 | t0119 | g0032 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19080 | hp2 | a0002 | c0002 | t0084 | g0259 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19082 | hp1 | a0001 | c0001 | t0011 | g0153 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19082 | hp2 | a0001 | c0001 | t0076 | g0203 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19085 | hp2 | a0006 | c0006 | t0007 | g0151 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19088 | hp1 | a0002 | c0003 | t0057 | g0360 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19088 | hp2 | a0001 | c0001 | t0018 | g0187 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19090 | hp1 | a0006 | c0006 | t0139 | g0132 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19090 | hp2 | a0001 | c0001 | t0028 | g0047 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19091 | hp1 | a0001 | c0001 | t0009 | g0056 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19091 | hp2 | a0001 | c0001 | t0024 | g0098 | EAS | JPT | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19240 | hp1 | a0002 | c0003 | t0006 | g0234 | AFR | YRI | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA19240 | hp2 | a0005 | c0007 | t0006 | g0335 | AFR | YRI | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA20129 | hp1 | a0002 | c0003 | t0134 | g0237 | AFR | ASW | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA20129 | hp2 | a0002 | c0003 | t0059 | g0362 | AFR | ASW | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0095 | EUR | TSI | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA20752 | hp2 | a0002 | c0002 | t0008 | g0058 | EUR | TSI | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA20805 | hp1 | a0001 | c0001 | t0103 | g0089 | EUR | TSI | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA20805 | hp2 | a0002 | c0002 | t0013 | g0313 | EUR | TSI | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA20905 | hp1 | a0001 | c0001 | t0013 | g0163 | SAS | GIH | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0330 | SAS | GIH | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01123 | hp1 | a0002 | c0002 | t0003 | g0294 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02109 | hp1 | a0002 | c0003 | t0016 | g0339 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02109 | hp2 | a0002 | c0003 | t0144 | g0072 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02559 | hp1 | a0001 | c0001 | t0124 | g0185 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG02559 | hp2 | a0002 | c0003 | t0046 | g0064 | AFR | ACB | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03471 | hp1 | a0002 | c0003 | t0015 | g0342 | AFR | MSL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG03471 | hp2 | a0009 | c0012 | t0082 | g0284 | AFR | MSL | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG06807 | hp1 | a0002 | c0002 | t0005 | g0327 | AFR | USA | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
HG06807 | hp2 | a0004 | c0005 | t0106 | g0184 | AFR | USA | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA20300 | hp1 | a0002 | c0002 | t0020 | g0246 | AFR | USA | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
NA20300 | hp2 | a0001 | c0001 | t0087 | g0004 | AFR | USA | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
homoSapiens | chm13v2 | a0001 | c0001 | t0072 | g0219 | REF | REF | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0120 | REF | REF | SCIN_chr7_12565720_12665182 | SCIN | chr7 | 12565720 | 12665182 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:12570789 | G | T | 1 | a0014 | 1 | HG02083.hp1 | start_lost | HIGH | c.3G>T | p.Met1? | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/16 | 70/9682 | 3/2148 | 1/715 | chr7 | 12570789 | |||
chr7:12570952 | C | T | 1 | a0007 | 6 | NA18951.hp2 NA18966.hp2 NA18977.hp1 others(3): Show |
stop_gained | HIGH | c.166C>T | p.Arg56* | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/16 | 233/9682 | 166/2148 | 56/715 | chr7 | 12570952 | |||
chr7:12570968 | A | G | 8 | a0002 a0005 a0009 others(5): Show |
143 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(140): Show |
missense_variant | MODERATE | c.182A>G | p.His61Arg | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/16 | 249/9682 | 182/2148 | 61/715 | chr7 | 12570968 | |||
chr7:12578152 | T | A | 1 | a0012 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.288T>A | p.Asn96Lys | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/16 | 355/9682 | 288/2148 | 96/715 | chr7 | 12578152 | |||
chr7:12581165 | C | G | 1 | a0008 | 4 | HG02723.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
missense_variant | MODERATE | c.460C>G | p.Pro154Ala | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/16 | 527/9682 | 460/2148 | 154/715 | chr7 | 12581165 | |||
chr7:12604628 | G | A | 1 | a0006 | 6 | NA18940.hp1 NA18945.hp1 NA18993.hp1 others(3): Show |
missense_variant | MODERATE | c.631G>A | p.Val211Met | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/16 | 698/9682 | 631/2148 | 211/715 | chr7 | 12604628 | |||
chr7:12626663 | A | G | 1 | a0017 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1061A>G | p.Asp354Gly | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/16 | 1128/9682 | 1061/2148 | 354/715 | chr7 | 12626663 | |||
chr7:12629135 | T | A | 1 | a0013 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.1232T>A | p.Val411Asp | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/16 | 1299/9682 | 1232/2148 | 411/715 | chr7 | 12629135 | |||
chr7:12636052 | G | C | 1 | a0005 | 6 | HG02145.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
missense_variant | MODERATE | c.1327G>C | p.Ala443Pro | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/16 | 1394/9682 | 1327/2148 | 443/715 | chr7 | 12636052 | |||
chr7:12636065 | G | A | 2 | a0004 a0011 |
9 | HG00738.hp1 HG00741.hp2 HG01975.hp1 others(6): Show |
missense_variant | MODERATE | c.1340G>A | p.Arg447Gln | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/16 | 1407/9682 | 1340/2148 | 447/715 | chr7 | 12636065 | |||
chr7:12636073 | C | A | 1 | a0019 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.1348C>A | p.Leu450Met | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/16 | 1415/9682 | 1348/2148 | 450/715 | chr7 | 12636073 | |||
chr7:12636088 | T | C | 3 | a0004 a0011 a0016 |
10 | HG00738.hp1 HG00741.hp2 HG01975.hp1 others(7): Show |
missense_variant | MODERATE | c.1363T>C | p.Phe455Leu | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/16 | 1430/9682 | 1363/2148 | 455/715 | chr7 | 12636088 | |||
chr7:12636110 | G | A | 1 | a0010 | 3 | HG02896.hp2 HG02897.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.1385G>A | p.Arg462Gln | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/16 | 1452/9682 | 1385/2148 | 462/715 | chr7 | 12636110 | |||
chr7:12640435 | A | G | 1 | a0009 | 3 | HG02257.hp2 HG03453.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.1499A>G | p.Lys500Arg | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/16 | 1566/9682 | 1499/2148 | 500/715 | chr7 | 12640435 | |||
chr7:12640483 | G | A | 1 | a0018 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.1547G>A | p.Arg516Gln | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/16 | 1614/9682 | 1547/2148 | 516/715 | chr7 | 12640483 | |||
chr7:12649512 | G | A | 3 | a0003 a0007 a0015 |
12 | HG00735.hp1 HG01069.hp1 HG01070.hp1 others(9): Show |
missense_variant | MODERATE | c.1927G>A | p.Asp643Asn | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/16 | 1994/9682 | 1927/2148 | 643/715 | chr7 | 12649512 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:12570825 | G | A | 1 | a0002c0010 | 3 | HG01106.hp2 HG01952.hp2 HG03491.hp1 |
synonymous_variant | LOW | c.39G>A | p.Ala13Ala | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/16 | 106/9682 | 39/2148 | 13/715 | chr7 | 12570825 | |||
chr7:12581179 | C | T | 7 | a0002c0002 a0002c0010 a0009c0012 others(4): Show |
92 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(89): Show |
synonymous_variant | LOW | c.474C>T | p.Asp158Asp | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/16 | 541/9682 | 474/2148 | 158/715 | chr7 | 12581179 | |||
chr7:12626793 | A | G | 1 | a0002c0019 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.1191A>G | p.Lys397Lys | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/16 | 1258/9682 | 1191/2148 | 397/715 | chr7 | 12626793 | |||
chr7:12636060 | C | T | 1 | a0002c0014 | 2 | HG02717.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.1335C>T | p.Ala445Ala | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/16 | 1402/9682 | 1335/2148 | 445/715 | chr7 | 12636060 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:12570747 | G | A | 7 | a0001c0001t0050 a0001c0001t0051 a0001c0001t0052 others(4): Show |
7 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-40G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/16 | 40 | chr7 | 12570747 | ||||||
chr7:12570753 | T | C | 9 | a0002c0003t0056 a0002c0003t0057 a0002c0003t0058 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-34T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/16 | 34 | chr7 | 12570753 | ||||||
chr7:12652879 | G | A | 34 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(31): Show |
66 | HG00544.hp2 HG01069.hp1 HG01069.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*164G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 164 | chr7 | 12652879 | ||||||
chr7:12652931 | C | T | 6 | a0001c0001t0185 a0002c0003t0046 a0002c0003t0047 others(3): Show |
8 | HG02451.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*216C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 216 | chr7 | 12652931 | ||||||
chr7:12652997 | T | G | 3 | a0002c0002t0079 a0005c0007t0081 a0009c0012t0080 |
3 | HG02145.hp1 HG02572.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*282T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 282 | chr7 | 12652997 | ||||||
chr7:12653086 | C | G | 1 | a0001c0001t0183 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 371 | chr7 | 12653086 | ||||||
chr7:12653100 | C | CA | 23 | a0001c0001t0027 a0001c0001t0066 a0001c0001t0086 others(20): Show |
26 | HG00423.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*405dupA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 406 | INFO_REALIGN_3_PRIME | chr7 | 12653100 | |||||
chr7:12653100 | C | CAAA | 9 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0083 others(6): Show |
12 | HG01109.hp2 HG02922.hp2 HG02970.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*403_*405dupAAA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 406 | INFO_REALIGN_3_PRIME | chr7 | 12653100 | |||||
chr7:12653100 | CA | C | 11 | a0001c0001t0020 a0001c0001t0076 a0001c0001t0179 others(8): Show |
13 | HG00099.hp1 HG01168.hp1 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*405delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 405 | INFO_REALIGN_3_PRIME | chr7 | 12653100 | |||||
chr7:12653184 | G | C | 1 | a0001c0001t0096 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*469G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 469 | chr7 | 12653184 | ||||||
chr7:12653313 | A | G | 50 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0014 others(47): Show |
79 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*598A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 598 | chr7 | 12653313 | ||||||
chr7:12653324 | T | C | 1 | a0001c0001t0097 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*609T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 609 | chr7 | 12653324 | ||||||
chr7:12653435 | CA | C | 3 | a0002c0002t0079 a0005c0007t0081 a0009c0012t0080 |
3 | HG02145.hp1 HG02572.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*724delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 724 | INFO_REALIGN_3_PRIME | chr7 | 12653435 | |||||
chr7:12653515 | A | G | 148 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(145): Show |
232 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*800A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 800 | chr7 | 12653515 | ||||||
chr7:12653543 | G | A | 2 | a0002c0002t0041 a0002c0002t0157 |
3 | HG00642.hp1 HG01243.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*828G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 828 | chr7 | 12653543 | ||||||
chr7:12653579 | C | G | 4 | a0002c0003t0134 a0005c0007t0034 a0010c0011t0135 others(1): Show |
4 | HG02976.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*864C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 864 | chr7 | 12653579 | ||||||
chr7:12653610 | T | G | 8 | a0001c0001t0011 a0001c0001t0028 a0001c0001t0099 others(5): Show |
11 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*895T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 895 | chr7 | 12653610 | ||||||
chr7:12653655 | A | T | 1 | a0001c0001t0176 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*940A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 940 | chr7 | 12653655 | ||||||
chr7:12653767 | C | T | 28 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0024 others(25): Show |
43 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1052C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 1052 | chr7 | 12653767 | ||||||
chr7:12653808 | G | C | 1 | a0016c0016t0148 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1093G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 1093 | chr7 | 12653808 | ||||||
chr7:12653907 | C | A | 1 | a0002c0002t0158 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1192C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 1192 | chr7 | 12653907 | ||||||
chr7:12654013 | T | C | 12 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0083 others(9): Show |
15 | HG01109.hp2 HG02809.hp1 HG02922.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1298T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 1298 | chr7 | 12654013 | ||||||
chr7:12654064 | T | C | 3 | a0001c0001t0101 a0002c0002t0098 a0002c0002t0177 |
3 | HG00558.hp2 NA18747.hp1 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1349T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 1349 | chr7 | 12654064 | ||||||
chr7:12654300 | A | C | 2 | a0001c0001t0132 a0001c0001t0133 |
2 | HG01081.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1585A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 1585 | chr7 | 12654300 | ||||||
chr7:12654458 | T | C | 151 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(148): Show |
235 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*1743T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 1743 | chr7 | 12654458 | ||||||
chr7:12654510 | G | C | 3 | a0001c0001t0136 a0008c0009t0159 a0008c0009t0160 |
3 | HG02809.hp1 HG03486.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1795G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 1795 | chr7 | 12654510 | ||||||
chr7:12654590 | G | C | 1 | a0001c0001t0067 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1875G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 1875 | chr7 | 12654590 | ||||||
chr7:12654733 | C | T | 1 | a0007c0008t0147 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2018C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2018 | chr7 | 12654733 | ||||||
chr7:12654768 | G | A | 1 | a0002c0003t0161 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2053G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2053 | chr7 | 12654768 | ||||||
chr7:12654801 | G | A | 28 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0024 others(25): Show |
43 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2086G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2086 | chr7 | 12654801 | ||||||
chr7:12654811 | C | T | 47 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0014 others(44): Show |
76 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2096C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2096 | chr7 | 12654811 | ||||||
chr7:12654922 | C | T | 30 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0024 others(27): Show |
45 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2207C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2207 | chr7 | 12654922 | ||||||
chr7:12654929 | G | T | 2 | a0001c0001t0022 a0002c0003t0022 |
3 | HG03490.hp1 HG03492.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2214G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2214 | chr7 | 12654929 | ||||||
chr7:12654938 | A | G | 6 | a0001c0001t0185 a0002c0003t0046 a0002c0003t0047 others(3): Show |
8 | HG02451.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2223A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2223 | chr7 | 12654938 | ||||||
chr7:12654979 | A | C | 12 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0083 others(9): Show |
15 | HG01109.hp2 HG02809.hp1 HG02922.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2264A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2264 | chr7 | 12654979 | ||||||
chr7:12655014 | G | A | 16 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0029 others(13): Show |
21 | HG01167.hp2 HG01891.hp2 HG02027.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2299G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2299 | chr7 | 12655014 | ||||||
chr7:12655112 | T | C | 26 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0018 others(23): Show |
33 | HG01167.hp2 HG01891.hp2 HG02027.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2397T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2397 | chr7 | 12655112 | ||||||
chr7:12655164 | T | G | 1 | a0001c0001t0030 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2449T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2449 | chr7 | 12655164 | ||||||
chr7:12655206 | T | A | 47 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0014 others(44): Show |
76 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2491T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2491 | chr7 | 12655206 | ||||||
chr7:12655376 | T | A | 10 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0083 others(7): Show |
13 | HG01109.hp2 HG02922.hp2 HG02970.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2661T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2661 | chr7 | 12655376 | ||||||
chr7:12655544 | A | G | 62 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(59): Show |
99 | HG00544.hp2 HG01069.hp1 HG01069.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2829A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 2829 | chr7 | 12655544 | ||||||
chr7:12655779 | T | C | 6 | a0001c0001t0185 a0002c0003t0046 a0002c0003t0047 others(3): Show |
8 | HG02451.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3064T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3064 | chr7 | 12655779 | ||||||
chr7:12655817 | T | C | 48 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0014 others(45): Show |
77 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3102T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3102 | chr7 | 12655817 | ||||||
chr7:12655873 | A | C | 2 | a0008c0009t0159 a0008c0009t0160 |
2 | HG02809.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3158A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3158 | chr7 | 12655873 | ||||||
chr7:12655882 | A | G | 62 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(59): Show |
99 | HG00544.hp2 HG01069.hp1 HG01069.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*3167A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3167 | chr7 | 12655882 | ||||||
chr7:12655899 | G | A | 1 | a0001c0001t0163 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3184G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3184 | chr7 | 12655899 | ||||||
chr7:12655937 | C | T | 3 | a0002c0002t0079 a0005c0007t0081 a0009c0012t0080 |
3 | HG02145.hp1 HG02572.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3222C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3222 | chr7 | 12655937 | ||||||
chr7:12655948 | G | T | 1 | a0001c0001t0040 | 2 | HG01070.hp2 HG01081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3233G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3233 | chr7 | 12655948 | ||||||
chr7:12656065 | T | A | 150 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(147): Show |
234 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*3350T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3350 | chr7 | 12656065 | ||||||
chr7:12656218 | T | A | 10 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0083 others(7): Show |
13 | HG01109.hp2 HG02922.hp2 HG02970.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3503T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3503 | chr7 | 12656218 | ||||||
chr7:12656289 | C | G | 2 | a0008c0009t0159 a0008c0009t0160 |
2 | HG02809.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3574C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3574 | chr7 | 12656289 | ||||||
chr7:12656307 | A | C | 46 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0014 others(43): Show |
75 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*3592A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3592 | chr7 | 12656307 | ||||||
chr7:12656310 | C | A | 16 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0029 others(13): Show |
21 | HG01167.hp2 HG01891.hp2 HG02027.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3595C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3595 | chr7 | 12656310 | ||||||
chr7:12656372 | T | G | 28 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0024 others(25): Show |
43 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3657T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3657 | chr7 | 12656372 | ||||||
chr7:12656404 | TATTTATT others(9): Show |
T | 1 | a0001c0001t0107 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3714_*3729delTAAA others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3714 | INFO_REALIGN_3_PRIME | chr7 | 12656404 | |||||
chr7:12656539 | C | A | 3 | a0002c0002t0079 a0005c0007t0081 a0009c0012t0080 |
3 | HG02145.hp1 HG02572.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3824C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3824 | chr7 | 12656539 | ||||||
chr7:12656659 | G | C | 7 | a0001c0001t0014 a0001c0001t0166 a0002c0002t0180 others(4): Show |
8 | HG01255.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3944G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3944 | chr7 | 12656659 | ||||||
chr7:12656674 | A | C | 1 | a0001c0001t0131 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3959A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3959 | chr7 | 12656674 | ||||||
chr7:12656680 | T | C | 10 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0083 others(7): Show |
13 | HG01109.hp2 HG02922.hp2 HG02970.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3965T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 3965 | chr7 | 12656680 | ||||||
chr7:12656728 | C | T | 2 | a0002c0002t0129 a0002c0002t0130 |
2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4013C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4013 | chr7 | 12656728 | ||||||
chr7:12656729 | C | G | 2 | a0005c0007t0034 a0017c0022t0034 |
2 | HG03195.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4014C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4014 | chr7 | 12656729 | ||||||
chr7:12656753 | C | G | 9 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0083 others(6): Show |
12 | HG01109.hp2 HG02922.hp2 HG02970.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4038C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4038 | chr7 | 12656753 | ||||||
chr7:12656781 | G | A | 2 | a0001c0001t0108 a0001c0001t0109 |
2 | HG03017.hp1 HG03654.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4066G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4066 | chr7 | 12656781 | ||||||
chr7:12656795 | C | T | 1 | a0008c0009t0160 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4080C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4080 | chr7 | 12656795 | ||||||
chr7:12656927 | GA | G | 6 | a0002c0002t0015 a0002c0002t0156 a0002c0002t0175 others(3): Show |
8 | HG03471.hp1 HG03540.hp1 HG03834.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4222delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4222 | INFO_REALIGN_3_PRIME | chr7 | 12656927 | |||||
chr7:12656968 | A | G | 2 | a0001c0001t0073 a0002c0003t0057 |
2 | NA18970.hp2 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4253A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4253 | chr7 | 12656968 | ||||||
chr7:12657095 | A | G | 33 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(30): Show |
63 | HG00642.hp2 HG01069.hp1 HG01069.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*4380A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4380 | chr7 | 12657095 | ||||||
chr7:12657164 | G | A | 21 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0112 others(18): Show |
24 | HG01243.hp1 HG01255.hp2 HG02280.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4449G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4449 | chr7 | 12657164 | ||||||
chr7:12657211 | A | AT | 42 | a0001c0001t0009 a0001c0001t0017 a0001c0001t0023 others(39): Show |
51 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*4521dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4522 | INFO_REALIGN_3_PRIME | chr7 | 12657211 | |||||
chr7:12657211 | A | ATT | 24 | a0001c0001t0014 a0001c0001t0021 a0001c0001t0076 others(21): Show |
29 | HG00438.hp1 HG01168.hp1 HG02258.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4520_*4521dupTT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4522 | INFO_REALIGN_3_PRIME | chr7 | 12657211 | |||||
chr7:12657211 | A | ATTT | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0022 others(20): Show |
48 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*4519_*4521dupTTT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4522 | INFO_REALIGN_3_PRIME | chr7 | 12657211 | |||||
chr7:12657211 | AT | A | 34 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0019 others(31): Show |
43 | HG00323.hp2 HG00738.hp1 HG01070.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*4521delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4521 | INFO_REALIGN_3_PRIME | chr7 | 12657211 | |||||
chr7:12657211 | ATT | A | 10 | a0001c0001t0141 a0002c0002t0031 a0002c0002t0084 others(7): Show |
10 | HG01243.hp1 HG01255.hp2 HG02145.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4520_*4521delTT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4520 | INFO_REALIGN_3_PRIME | chr7 | 12657211 | |||||
chr7:12657211 | ATTT | A | 6 | a0001c0001t0112 a0001c0001t0136 a0002c0002t0079 others(3): Show |
6 | HG02572.hp2 HG02602.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4519_*4521delTTT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4519 | INFO_REALIGN_3_PRIME | chr7 | 12657211 | |||||
chr7:12657211 | ATTTTT | A | 9 | a0001c0001t0006 a0001c0001t0050 a0002c0003t0006 others(6): Show |
12 | HG02723.hp2 HG02922.hp2 HG02970.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4517_*4521delTTTT others(1): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4517 | INFO_REALIGN_3_PRIME | chr7 | 12657211 | |||||
chr7:12657373 | C | T | 1 | a0001c0001t0124 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4658C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4658 | chr7 | 12657373 | ||||||
chr7:12657480 | AT | A | 9 | a0002c0002t0031 a0002c0002t0113 a0002c0003t0134 others(6): Show |
9 | HG01243.hp1 HG01255.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4767delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4767 | INFO_REALIGN_3_PRIME | chr7 | 12657480 | |||||
chr7:12657487 | G | T | 1 | a0001c0001t0112 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4772G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4772 | chr7 | 12657487 | ||||||
chr7:12657538 | G | GTA | 3 | a0001c0001t0074 a0001c0001t0097 a0001c0001t0170 |
3 | NA18939.hp1 NA18956.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4857_*4858dupAT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657538 | |||||
chr7:12657538 | G | GTATA | 4 | a0001c0001t0103 a0001c0001t0118 a0001c0001t0131 others(1): Show |
4 | HG00544.hp1 HG03669.hp2 NA18968.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4855_*4858dupATAT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657538 | |||||
chr7:12657538 | G | GTATATA | 5 | a0001c0001t0055 a0001c0001t0099 a0001c0001t0153 others(2): Show |
5 | HG00741.hp1 HG01496.hp2 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4853_*4858dupATAT others(2): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657538 | |||||
chr7:12657538 | G | GTATATAT others(1): Show |
3 | a0001c0001t0035 a0001c0001t0102 a0001c0001t0152 |
4 | HG01891.hp2 HG02135.hp1 NA18946.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4851_*4858dupATAT others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657538 | |||||
chr7:12657538 | G | GTATATAT others(3): Show |
2 | a0001c0001t0024 a0002c0002t0091 |
4 | HG01978.hp2 HG02040.hp2 NA18951.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4849_*4858dupATAT others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657538 | |||||
chr7:12657538 | G | GTATATAT others(5): Show |
5 | a0001c0001t0117 a0001c0001t0125 a0001c0001t0137 others(2): Show |
6 | HG02559.hp2 HG03139.hp1 NA18981.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4847_*4858dupATAT others(8): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657538 | |||||
chr7:12657538 | G | GTATATAT others(7): Show |
2 | a0001c0001t0027 a0001c0001t0116 |
3 | HG01167.hp1 HG01169.hp2 NA18970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4845_*4858dupATAT others(10): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657538 | |||||
chr7:12657538 | G | GTATATAT others(9): Show |
1 | a0001c0001t0054 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4843_*4858dupATAT others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657538 | |||||
chr7:12657538 | GTA | G | 12 | a0001c0001t0013 a0001c0001t0016 a0001c0001t0108 others(9): Show |
14 | HG00099.hp2 HG00544.hp2 HG01261.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4857_*4858delAT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4857 | INFO_REALIGN_3_PRIME | chr7 | 12657538 | |||||
chr7:12657539 | T | C | 1 | a0002c0003t0056 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4824T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4824 | chr7 | 12657539 | ||||||
chr7:12657540 | A | G | 14 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0100 others(11): Show |
16 | HG00673.hp2 HG01243.hp1 HG01255.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4825A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4825 | chr7 | 12657540 | ||||||
chr7:12657544 | A | G | 2 | a0001c0001t0141 a0010c0011t0135 |
2 | HG02280.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4829A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4829 | chr7 | 12657544 | ||||||
chr7:12657548 | A | G | 1 | a0001c0001t0141 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4833A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4833 | chr7 | 12657548 | ||||||
chr7:12657556 | ATATATAT others(10): Show |
A | 1 | a0002c0003t0146 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4843_*4859delATAT others(13): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4843 | INFO_REALIGN_3_PRIME | chr7 | 12657556 | |||||
chr7:12657556 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0145 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4843_*4860delATAT others(14): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4843 | INFO_REALIGN_3_PRIME | chr7 | 12657556 | |||||
chr7:12657556 | ATATATAT others(15): Show |
A | 2 | a0001c0001t0042 a0004c0005t0042 |
2 | HG00741.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4843_*4864delATAT others(18): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4843 | INFO_REALIGN_3_PRIME | chr7 | 12657556 | |||||
chr7:12657556 | ATATATAT others(16): Show |
A | 1 | a0016c0016t0148 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4843_*4865delATAT others(19): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4843 | INFO_REALIGN_3_PRIME | chr7 | 12657556 | |||||
chr7:12657557 | T | C | 11 | a0001c0001t0006 a0001c0001t0050 a0002c0003t0006 others(8): Show |
14 | HG02109.hp2 HG02723.hp2 HG02922.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4842T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4842 | chr7 | 12657557 | ||||||
chr7:12657560 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0133 a0001c0001t0141 |
2 | HG02280.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4847_*4859delATAT others(9): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4847 | INFO_REALIGN_3_PRIME | chr7 | 12657560 | |||||
chr7:12657560 | ATATATAT others(8): Show |
A | 1 | a0002c0003t0161 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4847_*4861delATAT others(11): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4847 | INFO_REALIGN_3_PRIME | chr7 | 12657560 | |||||
chr7:12657560 | ATATATAT others(9): Show |
A | 1 | a0003c0004t0004 | 3 | NA18965.hp1 NA18982.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4847_*4862delATAT others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4847 | INFO_REALIGN_3_PRIME | chr7 | 12657560 | |||||
chr7:12657562 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0004 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4849_*4862delATAT others(10): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4849 | INFO_REALIGN_3_PRIME | chr7 | 12657562 | |||||
chr7:12657562 | ATATATAT others(9): Show |
A | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0073 others(7): Show |
13 | HG01069.hp1 HG01123.hp1 HG01192.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4849_*4864delATAT others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4849 | INFO_REALIGN_3_PRIME | chr7 | 12657562 | |||||
chr7:12657562 | ATATATAT others(10): Show |
A | 4 | a0001c0001t0003 a0001c0001t0017 a0002c0002t0077 others(1): Show |
6 | HG01516.hp1 HG01517.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4849_*4865delATAT others(13): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4849 | INFO_REALIGN_3_PRIME | chr7 | 12657562 | |||||
chr7:12657562 | ATATATAT others(11): Show |
A | 3 | a0001c0001t0121 a0002c0002t0010 a0002c0003t0017 |
5 | HG02145.hp2 HG02257.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4849_*4866delATAT others(14): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4849 | INFO_REALIGN_3_PRIME | chr7 | 12657562 | |||||
chr7:12657564 | ATATATAT others(4): Show |
A | 1 | a0002c0002t0018 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4851_*4861delATAT others(7): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4851 | INFO_REALIGN_3_PRIME | chr7 | 12657564 | |||||
chr7:12657564 | ATATATAT others(9): Show |
A | 13 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0021 others(10): Show |
23 | HG01099.hp2 HG02132.hp1 HG02451.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4851_*4866delATAT others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4851 | INFO_REALIGN_3_PRIME | chr7 | 12657564 | |||||
chr7:12657564 | ATATATAT others(10): Show |
A | 7 | a0001c0001t0022 a0001c0001t0043 a0002c0002t0015 others(4): Show |
11 | HG01433.hp2 HG01884.hp1 HG03471.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4851_*4867delATAT others(13): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4851 | INFO_REALIGN_3_PRIME | chr7 | 12657564 | |||||
chr7:12657564 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0010 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4851_*4868delATAT others(14): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4851 | INFO_REALIGN_3_PRIME | chr7 | 12657564 | |||||
chr7:12657565 | T | C | 1 | a0001c0001t0136 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4850T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4850 | chr7 | 12657565 | ||||||
chr7:12657566 | A | T | 1 | a0001c0001t0123 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4851A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4851 | chr7 | 12657566 | ||||||
chr7:12657566 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0003 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4853_*4866delATAT others(10): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4853 | INFO_REALIGN_3_PRIME | chr7 | 12657566 | |||||
chr7:12657566 | ATATATAT others(8): Show |
A | 3 | a0001c0001t0003 a0002c0002t0003 a0002c0003t0089 |
4 | HG01069.hp2 HG01071.hp2 HG01346.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4853_*4867delATAT others(11): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4853 | INFO_REALIGN_3_PRIME | chr7 | 12657566 | |||||
chr7:12657566 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0070 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4853_*4868delATAT others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4853 | INFO_REALIGN_3_PRIME | chr7 | 12657566 | |||||
chr7:12657568 | A | T | 2 | a0001c0001t0123 a0002c0002t0016 |
2 | HG02027.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4853A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4853 | chr7 | 12657568 | ||||||
chr7:12657569 | TA | T | 4 | a0001c0001t0019 a0001c0001t0051 a0001c0001t0154 others(1): Show |
5 | HG00323.hp2 HG01175.hp1 HG01175.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4855delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4855 | chr7 | 12657569 | ||||||
chr7:12657570 | A | AT | 4 | a0001c0001t0014 a0001c0001t0040 a0002c0002t0180 others(1): Show |
5 | HG01070.hp2 HG01081.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4856dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4857 | INFO_REALIGN_3_PRIME | chr7 | 12657570 | |||||
chr7:12657570 | A | T | 11 | a0001c0001t0019 a0001c0001t0093 a0001c0001t0123 others(8): Show |
11 | HG00738.hp1 HG01255.hp1 HG02027.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4855A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4855 | chr7 | 12657570 | ||||||
chr7:12657570 | ATATTTTT others(8): Show |
A | 1 | a0002c0014t0006 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4857_*4871delATTT others(11): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4857 | INFO_REALIGN_3_PRIME | chr7 | 12657570 | |||||
chr7:12657570 | ATATTTTT others(9): Show |
A | 2 | a0008c0009t0110 a0009c0012t0082 |
2 | HG02723.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4857_*4872delATTT others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4857 | INFO_REALIGN_3_PRIME | chr7 | 12657570 | |||||
chr7:12657571 | TA | T | 5 | a0001c0001t0166 a0002c0002t0012 a0002c0002t0129 others(2): Show |
6 | HG01257.hp1 HG01258.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4857delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4857 | chr7 | 12657571 | ||||||
chr7:12657572 | A | ATATATAT | 4 | a0001c0001t0011 a0001c0001t0052 a0001c0001t0053 others(1): Show |
6 | HG01256.hp2 HG01258.hp2 NA18964.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(3): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(8): Show |
1 | a0002c0002t0008 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(11): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(10): Show |
1 | a0001c0001t0030 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(13): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(19): Show |
1 | a0002c0002t0175 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(22): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(20): Show |
2 | a0002c0002t0008 a0002c0003t0002 |
2 | HG01993.hp2 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(23): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(12): Show |
1 | a0002c0002t0002 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(15): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(15): Show |
1 | a0001c0001t0002 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(18): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(17): Show |
1 | a0001c0001t0002 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(20): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(18): Show |
1 | a0001c0001t0071 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(21): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(9): Show |
3 | a0001c0001t0002 a0002c0002t0002 a0012c0018t0002 |
3 | HG00140.hp1 HG01496.hp1 NA18987.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(10): Show |
1 | a0002c0002t0002 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(13): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(11): Show |
1 | a0001c0001t0002 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(14): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(12): Show |
3 | a0002c0002t0002 a0002c0002t0026 a0002c0002t0041 |
3 | HG00642.hp1 HG02015.hp1 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(15): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(13): Show |
3 | a0002c0002t0002 a0002c0002t0041 a0002c0002t0167 |
3 | HG01243.hp2 HG02698.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(16): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(9): Show |
1 | a0001c0001t0005 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(10): Show |
3 | a0001c0001t0002 a0001c0001t0044 a0002c0002t0002 |
3 | HG02258.hp2 HG04199.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(13): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(11): Show |
1 | a0001c0001t0005 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(14): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(13): Show |
1 | a0001c0001t0002 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(16): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(11): Show |
1 | a0001c0001t0100 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(14): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(6): Show |
1 | a0002c0002t0169 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(9): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(9): Show |
1 | a0002c0002t0157 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(12): Show |
1 | a0002c0002t0026 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(15): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(4): Show |
1 | a0002c0002t0002 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(7): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(5): Show |
1 | a0002c0002t0002 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(8): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(6): Show |
1 | a0007c0008t0009 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(9): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(7): Show |
1 | a0002c0002t0005 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(10): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(9): Show |
1 | a0002c0002t0182 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(10): Show |
1 | a0002c0003t0008 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(13): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(11): Show |
1 | a0002c0003t0008 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(14): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(12): Show |
1 | a0002c0002t0078 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(15): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(2): Show |
5 | a0001c0001t0009 a0001c0001t0045 a0002c0003t0058 others(2): Show |
6 | HG00408.hp1 HG00597.hp2 HG04184.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(5): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(3): Show |
6 | a0001c0001t0009 a0001c0001t0162 a0001c0001t0164 others(3): Show |
6 | HG02083.hp1 HG02280.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(4): Show |
2 | a0001c0001t0008 a0001c0001t0094 |
2 | HG00423.hp1 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(7): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(5): Show |
1 | a0001c0001t0023 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(8): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATAT others(8): Show |
1 | a0001c0001t0023 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(11): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATTT others(3): Show |
2 | a0001c0001t0009 a0001c0001t0095 |
2 | NA18983.hp2 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATTT others(4): Show |
1 | a0001c0001t0163 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(7): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATATTT others(6): Show |
1 | a0001c0001t0009 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(9): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATTTTT others(3): Show |
2 | a0002c0002t0156 a0007c0008t0039 |
2 | NA18966.hp1 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATTT others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATATTTTT others(4): Show |
2 | a0002c0002t0023 a0007c0023t0039 |
2 | NA18959.hp1 NA18991.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATTT others(7): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0176 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4874_*4883dupTTTT others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4884 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | A | T | 32 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0014 others(29): Show |
37 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*4857A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4857 | chr7 | 12657572 | ||||||
chr7:12657572 | AT | A | 8 | a0001c0001t0001 a0001c0001t0029 a0001c0001t0032 others(5): Show |
12 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4883delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4883 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657572 | ATTTTTTT others(8): Show |
A | 8 | a0001c0001t0006 a0001c0001t0050 a0002c0003t0006 others(5): Show |
11 | HG02109.hp2 HG02922.hp2 HG02970.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4869_*4883delTTTT others(11): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4869 | INFO_REALIGN_3_PRIME | chr7 | 12657572 | |||||
chr7:12657573 | T | TA | 3 | a0001c0001t0001 a0004c0005t0104 a0009c0012t0085 |
4 | HG02257.hp2 HG03831.hp1 HG04115.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | chr7 | 12657573 | ||||||
chr7:12657573 | T | TATATA | 3 | a0001c0001t0005 a0002c0002t0113 a0002c0003t0060 |
4 | HG03041.hp1 NA18954.hp2 NA18971.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(1): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | chr7 | 12657573 | ||||||
chr7:12657573 | T | TATATATA others(2): Show |
2 | a0001c0001t0018 a0007c0008t0147 |
3 | HG02165.hp1 NA18966.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(5): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | chr7 | 12657573 | ||||||
chr7:12657573 | T | TATATATA others(4): Show |
4 | a0001c0001t0005 a0002c0002t0001 a0002c0002t0005 others(1): Show |
6 | HG01515.hp1 HG01928.hp1 HG01928.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(7): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | chr7 | 12657573 | ||||||
chr7:12657573 | T | TATATATA others(6): Show |
6 | a0001c0001t0005 a0001c0001t0107 a0001c0001t0119 others(3): Show |
6 | HG01517.hp1 NA18945.hp1 NA19010.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(9): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | chr7 | 12657573 | ||||||
chr7:12657573 | T | TATATATA others(8): Show |
4 | a0001c0001t0001 a0001c0001t0096 a0001c0001t0115 others(1): Show |
4 | HG01943.hp2 NA18959.hp2 NA19002.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(11): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | chr7 | 12657573 | ||||||
chr7:12657573 | T | TATATATA others(10): Show |
1 | a0001c0001t0008 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4858_*4859insATAT others(13): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | chr7 | 12657573 | ||||||
chr7:12657574 | T | A | 24 | a0001c0001t0001 a0001c0001t0024 a0001c0001t0027 others(21): Show |
30 | HG00544.hp1 HG00741.hp1 HG01109.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4859T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4859 | chr7 | 12657574 | ||||||
chr7:12657575 | T | A | 19 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(16): Show |
25 | HG01928.hp1 HG01928.hp2 HG02080.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4860T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4860 | chr7 | 12657575 | ||||||
chr7:12657576 | T | A | 15 | a0001c0001t0001 a0001c0001t0024 a0001c0001t0035 others(12): Show |
17 | HG01496.hp2 HG01952.hp1 HG02135.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4861T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4861 | chr7 | 12657576 | ||||||
chr7:12657577 | T | A | 10 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0115 others(7): Show |
12 | HG01928.hp1 HG01928.hp2 HG02132.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4862T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4862 | chr7 | 12657577 | ||||||
chr7:12657578 | T | A | 7 | a0001c0001t0087 a0001c0001t0137 a0001c0001t0153 others(4): Show |
7 | HG01496.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4863T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4863 | chr7 | 12657578 | ||||||
chr7:12657579 | T | A | 4 | a0001c0001t0119 a0002c0002t0113 a0002c0003t0062 others(1): Show |
4 | HG03041.hp1 HG04115.hp2 NA19074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4864T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4864 | chr7 | 12657579 | ||||||
chr7:12657580 | T | A | 1 | a0001c0001t0153 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4865T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4865 | chr7 | 12657580 | ||||||
chr7:12657583 | T | A | 1 | a0001c0001t0136 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4868T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4868 | chr7 | 12657583 | ||||||
chr7:12657585 | T | A | 1 | a0001c0001t0136 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4870T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4870 | chr7 | 12657585 | ||||||
chr7:12657587 | T | A | 1 | a0001c0001t0136 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4872T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4872 | chr7 | 12657587 | ||||||
chr7:12657651 | T | G | 12 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0136 others(9): Show |
15 | HG02109.hp2 HG02723.hp2 HG02922.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4936T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 4936 | chr7 | 12657651 | ||||||
chr7:12657742 | C | G | 3 | a0002c0002t0079 a0005c0007t0081 a0009c0012t0080 |
3 | HG02145.hp1 HG02572.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5027C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5027 | chr7 | 12657742 | ||||||
chr7:12657838 | C | T | 86 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(83): Show |
135 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*5123C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5123 | chr7 | 12657838 | ||||||
chr7:12657874 | T | A | 12 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0136 others(9): Show |
15 | HG02109.hp2 HG02723.hp2 HG02922.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5159T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5159 | chr7 | 12657874 | ||||||
chr7:12657892 | A | T | 3 | a0001c0001t0133 a0002c0003t0089 a0002c0003t0161 |
3 | HG02258.hp1 NA18522.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5177A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5177 | chr7 | 12657892 | ||||||
chr7:12657925 | G | A | 12 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0136 others(9): Show |
15 | HG02109.hp2 HG02723.hp2 HG02922.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5210G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5210 | chr7 | 12657925 | ||||||
chr7:12657943 | A | C | 1 | a0002c0002t0169 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5228A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5228 | chr7 | 12657943 | ||||||
chr7:12657949 | C | G | 3 | a0001c0001t0141 a0005c0007t0034 a0017c0022t0034 |
3 | HG02280.hp1 HG03195.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5234C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5234 | chr7 | 12657949 | ||||||
chr7:12658005 | C | A | 4 | a0001c0001t0112 a0001c0001t0141 a0005c0007t0034 others(1): Show |
4 | HG02280.hp1 HG02602.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5290C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5290 | chr7 | 12658005 | ||||||
chr7:12658120 | T | A | 1 | a0001c0001t0124 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5405T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5405 | chr7 | 12658120 | ||||||
chr7:12658140 | A | T | 1 | a0001c0001t0124 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5425A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5425 | chr7 | 12658140 | ||||||
chr7:12658167 | C | T | 1 | a0002c0003t0089 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5452C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5452 | chr7 | 12658167 | ||||||
chr7:12658172 | A | C | 87 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(84): Show |
136 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*5457A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5457 | chr7 | 12658172 | ||||||
chr7:12658197 | A | G | 32 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0019 others(29): Show |
39 | HG00323.hp2 HG00544.hp2 HG00738.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*5482A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5482 | chr7 | 12658197 | ||||||
chr7:12658247 | A | G | 2 | a0008c0009t0159 a0008c0009t0160 |
2 | HG02809.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5532A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5532 | chr7 | 12658247 | ||||||
chr7:12658286 | A | G | 180 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(177): Show |
264 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*5571A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5571 | chr7 | 12658286 | ||||||
chr7:12658306 | C | G | 8 | a0001c0001t0014 a0001c0001t0166 a0001c0001t0185 others(5): Show |
10 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5591C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5591 | chr7 | 12658306 | ||||||
chr7:12658484 | A | C | 2 | a0002c0003t0134 a0010c0011t0135 |
2 | HG02976.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5769A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5769 | chr7 | 12658484 | ||||||
chr7:12658622 | G | C | 1 | a0001c0001t0120 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5907G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5907 | chr7 | 12658622 | ||||||
chr7:12658642 | G | A | 2 | a0001c0001t0102 a0001c0001t0105 |
2 | HG01167.hp2 HG01891.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5927G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 5927 | chr7 | 12658642 | ||||||
chr7:12658923 | C | A | 85 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(82): Show |
134 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*6208C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6208 | chr7 | 12658923 | ||||||
chr7:12658943 | GTTGTTGT | G | 11 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0136 others(8): Show |
14 | HG02723.hp2 HG02922.hp2 HG02970.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6234_*6240delGTTT others(3): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6234 | INFO_REALIGN_3_PRIME | chr7 | 12658943 | |||||
chr7:12658946 | G | A | 1 | a0002c0010t0001 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6231G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6231 | chr7 | 12658946 | ||||||
chr7:12659016 | C | G | 5 | a0002c0002t0031 a0002c0002t0113 a0002c0019t0064 others(2): Show |
5 | HG01243.hp1 HG01255.hp2 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6301C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6301 | chr7 | 12659016 | ||||||
chr7:12659059 | G | A | 12 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0124 others(9): Show |
15 | HG02559.hp1 HG02723.hp2 HG02922.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*6344G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6344 | chr7 | 12659059 | ||||||
chr7:12659110 | C | G | 11 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0136 others(8): Show |
14 | HG02723.hp2 HG02922.hp2 HG02970.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6395C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6395 | chr7 | 12659110 | ||||||
chr7:12659114 | C | T | 1 | a0001c0001t0093 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6399C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6399 | chr7 | 12659114 | ||||||
chr7:12659164 | G | A | 1 | a0002c0003t0089 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6449G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6449 | chr7 | 12659164 | ||||||
chr7:12659246 | G | A | 2 | a0002c0003t0134 a0010c0011t0135 |
2 | HG02976.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6531G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6531 | chr7 | 12659246 | ||||||
chr7:12659340 | C | A | 6 | a0001c0001t0044 a0001c0001t0094 a0001c0001t0122 others(3): Show |
6 | HG00423.hp1 HG02083.hp1 NA18939.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6625C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6625 | chr7 | 12659340 | ||||||
chr7:12659367 | G | A | 1 | a0001c0001t0066 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6652G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6652 | chr7 | 12659367 | ||||||
chr7:12659479 | A | T | 4 | a0001c0001t0045 a0001c0001t0095 a0001c0001t0162 others(1): Show |
5 | HG00408.hp1 HG00438.hp1 NA18945.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6764A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6764 | chr7 | 12659479 | ||||||
chr7:12659551 | G | C | 13 | a0001c0001t0006 a0001c0001t0050 a0001c0001t0136 others(10): Show |
16 | HG02723.hp2 HG02809.hp1 HG02922.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6836G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6836 | chr7 | 12659551 | ||||||
chr7:12659565 | A | G | 1 | a0001c0001t0124 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6850A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6850 | chr7 | 12659565 | ||||||
chr7:12659566 | T | C | 1 | a0002c0010t0128 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6851T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 6851 | chr7 | 12659566 | ||||||
chr7:12659826 | C | G | 9 | a0001c0001t0007 a0001c0001t0033 a0001c0001t0138 others(6): Show |
13 | HG00423.hp2 HG00558.hp1 HG01975.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7111C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 7111 | chr7 | 12659826 | ||||||
chr7:12659932 | G | C | 1 | a0001c0001t0124 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7217G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 7217 | chr7 | 12659932 | ||||||
chr7:12659951 | G | A | 177 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(174): Show |
261 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(258): Show |
3_prime_UTR_variant | MODIFIER | c.*7236G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 7236 | chr7 | 12659951 | ||||||
chr7:12659966 | TC | T | 7 | a0001c0001t0019 a0001c0001t0040 a0001c0001t0051 others(4): Show |
10 | HG00323.hp2 HG00738.hp1 HG01070.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7256delC | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 7256 | INFO_REALIGN_3_PRIME | chr7 | 12659966 | |||||
chr7:12659988 | T | C | 7 | a0001c0001t0093 a0001c0001t0112 a0001c0001t0133 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02602.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7273T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 16/16 | 7273 | chr7 | 12659988 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:12571015 | C | A | 48 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(45): Show |
48 | HG00099.hp1 HG00408.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.199+30C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571015 | |||||||
chr7:12571026 | C | T | 9 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.199+41C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571026 | |||||||
chr7:12571064 | G | C | 1 | a0002c0002t0008g0058 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.199+79G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571064 | |||||||
chr7:12571127 | G | A | 23 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(20): Show |
23 | HG00597.hp2 HG01255.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.199+142G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571127 | |||||||
chr7:12571183 | G | C | 48 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(45): Show |
48 | HG00099.hp1 HG00408.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.199+198G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571183 | |||||||
chr7:12571278 | C | T | 48 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(45): Show |
48 | HG00099.hp1 HG00408.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.199+293C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571278 | |||||||
chr7:12571307 | C | T | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.199+322C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571307 | |||||||
chr7:12571312 | C | G | 144 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(141): Show |
145 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.199+327C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571312 | |||||||
chr7:12571314 | G | C | 1 | a0001c0001t0007g0073 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.199+329G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571314 | |||||||
chr7:12571322 | A | G | 201 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.199+337A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571322 | |||||||
chr7:12571462 | A | G | 2 | a0002c0002t0001g0351 a0002c0002t0026g0352 |
2 | HG02015.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.199+477A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571462 | |||||||
chr7:12571554 | C | T | 7 | a0001c0001t0005g0229 a0001c0001t0019g0224 a0001c0001t0019g0230 others(4): Show |
7 | HG01070.hp2 HG01081.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.199+569C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571554 | |||||||
chr7:12571627 | T | C | 192 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.199+642T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571627 | |||||||
chr7:12571659 | T | G | 1 | a0002c0019t0064g0354 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.199+674T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571659 | |||||||
chr7:12571758 | G | T | 14 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(11): Show |
14 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.199+773G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571758 | |||||||
chr7:12571819 | C | A | 1 | a0001c0001t0170g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.199+834C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571819 | |||||||
chr7:12571850 | T | C | 1 | a0002c0002t0002g0239 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.199+865T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571850 | |||||||
chr7:12571928 | C | T | 48 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(45): Show |
48 | HG00099.hp1 HG00408.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.199+943C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571928 | |||||||
chr7:12571952 | C | G | 1 | a0005c0007t0034g0350 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.199+967C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12571952 | |||||||
chr7:12572001 | C | T | 14 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0003g0054 others(11): Show |
14 | HG00408.hp1 HG02015.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.199+1016C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12572001 | |||||||
chr7:12572007 | G | A | 23 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(20): Show |
23 | HG00597.hp2 HG01255.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.199+1022G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12572007 | |||||||
chr7:12572142 | A | G | 7 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(4): Show |
7 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+1157A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12572142 | |||||||
chr7:12572342 | T | C | 4 | a0008c0009t0006g0242 a0008c0009t0110g0240 a0008c0009t0159g0241 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1357T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12572342 | |||||||
chr7:12572387 | C | A | 1 | a0001c0001t0170g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.199+1402C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12572387 | |||||||
chr7:12572454 | A | G | 9 | a0002c0003t0006g0337 a0002c0003t0015g0340 a0002c0003t0015g0342 others(6): Show |
10 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.199+1469A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12572454 | |||||||
chr7:12572576 | C | T | 4 | a0001c0001t0003g0223 a0001c0001t0100g0222 a0002c0002t0012g0334 others(1): Show |
4 | HG00673.hp2 HG02922.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+1591C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12572576 | |||||||
chr7:12572744 | G | T | 4 | a0008c0009t0006g0242 a0008c0009t0110g0240 a0008c0009t0159g0241 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1759G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12572744 | |||||||
chr7:12573035 | G | A | 1 | a0001c0001t0019g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.199+2050G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573035 | |||||||
chr7:12573056 | T | C | 149 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(146): Show |
151 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.199+2071T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573056 | |||||||
chr7:12573108 | G | A | 48 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(45): Show |
48 | HG00099.hp1 HG00408.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.199+2123G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573108 | |||||||
chr7:12573116 | A | G | 1 | a0005c0007t0034g0350 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.199+2131A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573116 | |||||||
chr7:12573197 | T | A | 7 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(4): Show |
7 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+2212T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573197 | |||||||
chr7:12573320 | C | A | 7 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(4): Show |
7 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+2335C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573320 | |||||||
chr7:12573327 | G | T | 1 | a0001c0001t0017g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.199+2342G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573327 | |||||||
chr7:12573394 | G | A | 7 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(4): Show |
7 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+2409G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573394 | |||||||
chr7:12573434 | C | T | 92 | a0002c0002t0001g0252 a0002c0002t0001g0258 a0002c0002t0001g0260 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.199+2449C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573434 | |||||||
chr7:12573595 | C | G | 15 | a0002c0003t0006g0337 a0002c0003t0008g0249 a0002c0003t0008g0250 others(12): Show |
16 | HG01256.hp1 HG01261.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.199+2610C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573595 | |||||||
chr7:12573627 | C | T | 92 | a0002c0002t0001g0252 a0002c0002t0001g0258 a0002c0002t0001g0260 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.199+2642C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573627 | |||||||
chr7:12573639 | A | G | 52 | a0002c0002t0001g0304 a0002c0002t0001g0308 a0002c0002t0001g0311 others(49): Show |
52 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.199+2654A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573639 | |||||||
chr7:12573641 | C | A | 1 | a0001c0001t0120g0075 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.199+2656C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573641 | |||||||
chr7:12573741 | C | T | 1 | a0001c0001t0025g0218 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.199+2756C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573741 | |||||||
chr7:12573898 | G | A | 2 | a0002c0002t0001g0252 a0002c0002t0175g0251 |
2 | HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.199+2913G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12573898 | |||||||
chr7:12574058 | A | G | 48 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(45): Show |
48 | HG00099.hp1 HG00408.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.199+3073A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12574058 | |||||||
chr7:12574249 | G | T | 61 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(58): Show |
62 | HG00099.hp1 HG00408.hp1 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.199+3264G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12574249 | |||||||
chr7:12574422 | G | A | 4 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0002t0020g0246 others(1): Show |
4 | HG02280.hp2 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+3437G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12574422 | |||||||
chr7:12574534 | G | A | 9 | a0002c0003t0006g0337 a0002c0003t0015g0340 a0002c0003t0015g0342 others(6): Show |
10 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.200-3530G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12574534 | |||||||
chr7:12574557 | C | T | 9 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.200-3507C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12574557 | |||||||
chr7:12574617 | C | T | 1 | a0001c0001t0123g0057 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.200-3447C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12574617 | |||||||
chr7:12574736 | G | A | 59 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(56): Show |
60 | HG00099.hp1 HG00408.hp1 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.200-3328G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12574736 | |||||||
chr7:12574828 | C | A | 5 | a0002c0003t0006g0337 a0005c0007t0006g0335 a0005c0007t0047g0338 others(2): Show |
6 | HG02145.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.200-3236C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12574828 | |||||||
chr7:12574828 | C | T | 10 | a0001c0001t0009g0056 a0002c0003t0056g0358 a0002c0003t0057g0360 others(7): Show |
10 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.200-3236C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12574828 | |||||||
chr7:12574835 | C | T | 12 | a0002c0003t0006g0337 a0002c0003t0008g0249 a0002c0003t0008g0250 others(9): Show |
13 | HG01256.hp1 HG01261.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.200-3229C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12574835 | |||||||
chr7:12574840 | T | C | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.200-3224T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12574840 | |||||||
chr7:12575013 | A | C | 201 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.200-3051A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575013 | |||||||
chr7:12575162 | A | G | 2 | a0010c0011t0031g0005 a0010c0011t0111g0005 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.200-2902A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575162 | |||||||
chr7:12575173 | G | A | 1 | a0001c0001t0029g0076 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.200-2891G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575173 | |||||||
chr7:12575239 | C | CT | 10 | a0002c0003t0037g0071 a0002c0003t0056g0358 a0002c0003t0057g0360 others(7): Show |
10 | HG00597.hp2 HG01255.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.200-2813dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 12575239 | ||||||
chr7:12575307 | C | A | 7 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(4): Show |
7 | HG00597.hp2 HG02523.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.200-2757C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575307 | |||||||
chr7:12575339 | C | CT | 47 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(44): Show |
47 | HG00099.hp1 HG00408.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.200-2717dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 12575339 | ||||||
chr7:12575339 | CT | C | 11 | a0002c0003t0006g0234 a0002c0003t0006g0236 a0002c0003t0017g0231 others(8): Show |
12 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.200-2717delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 12575339 | ||||||
chr7:12575508 | G | T | 138 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(135): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.200-2556G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575508 | |||||||
chr7:12575704 | A | T | 1 | a0001c0001t0093g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.200-2360A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575704 | |||||||
chr7:12575708 | A | G | 22 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(19): Show |
22 | HG01167.hp2 HG01169.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.200-2356A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575708 | |||||||
chr7:12575772 | C | T | 2 | a0002c0003t0008g0249 a0002c0003t0008g0250 |
2 | HG01256.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.200-2292C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575772 | |||||||
chr7:12575810 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.200-2254A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575810 | |||||||
chr7:12575823 | T | C | 201 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.200-2241T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575823 | |||||||
chr7:12575824 | A | G | 1 | a0001c0001t0170g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.200-2240A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575824 | |||||||
chr7:12575906 | G | A | 1 | a0007c0008t0088g0077 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.200-2158G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575906 | |||||||
chr7:12575928 | G | A | 12 | a0002c0003t0006g0337 a0002c0003t0008g0249 a0002c0003t0008g0250 others(9): Show |
13 | HG01256.hp1 HG01261.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.200-2136G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575928 | |||||||
chr7:12575993 | T | C | 7 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(4): Show |
7 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.200-2071T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12575993 | |||||||
chr7:12576073 | C | T | 179 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(176): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.200-1991C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576073 | |||||||
chr7:12576147 | A | C | 179 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(176): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.200-1917A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576147 | |||||||
chr7:12576222 | G | A | 1 | a0001c0001t0003g0078 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.200-1842G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576222 | |||||||
chr7:12576234 | G | A | 18 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(15): Show |
19 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.200-1830G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576234 | |||||||
chr7:12576306 | A | G | 4 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0002t0020g0246 others(1): Show |
4 | HG02280.hp2 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.200-1758A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576306 | |||||||
chr7:12576358 | G | GT | 18 | a0001c0001t0001g0004 a0001c0001t0001g0214 a0001c0001t0003g0206 others(15): Show |
18 | HG00673.hp2 HG01361.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-1697dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 12576358 | ||||||
chr7:12576358 | GT | G | 65 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(62): Show |
65 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.200-1697delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 12576358 | ||||||
chr7:12576367 | TG | T | 133 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(130): Show |
135 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.200-1696delG | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576367 | |||||||
chr7:12576368 | G | T | 86 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0091 others(83): Show |
89 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.200-1696G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576368 | |||||||
chr7:12576378 | T | A | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.200-1686T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576378 | |||||||
chr7:12576504 | G | C | 201 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.200-1560G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576504 | |||||||
chr7:12576512 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.200-1552G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576512 | |||||||
chr7:12576514 | G | A | 34 | a0002c0003t0006g0063 a0002c0003t0006g0337 a0002c0003t0008g0249 others(31): Show |
35 | HG00597.hp2 HG01255.hp2 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.200-1550G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576514 | |||||||
chr7:12576558 | A | G | 57 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(54): Show |
59 | HG00597.hp2 HG00738.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.200-1506A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576558 | |||||||
chr7:12576617 | A | C | 4 | a0002c0003t0014g0069 a0002c0003t0037g0071 a0002c0003t0047g0070 others(1): Show |
4 | HG02451.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.200-1447A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576617 | |||||||
chr7:12576646 | A | G | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.200-1418A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576646 | |||||||
chr7:12576730 | TGACCTCA | T | 201 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.200-1331_200-1325d others(9): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 12576730 | ||||||
chr7:12576939 | C | T | 3 | a0002c0003t0008g0249 a0002c0003t0008g0250 a0002c0003t0022g0248 |
3 | HG01256.hp1 HG01261.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.200-1125C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576939 | |||||||
chr7:12576965 | G | C | 47 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0091 others(44): Show |
48 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.200-1099G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12576965 | |||||||
chr7:12577148 | T | G | 1 | a0001c0001t0014g0112 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.200-916T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12577148 | |||||||
chr7:12577169 | G | A | 2 | a0002c0002t0001g0351 a0002c0002t0026g0352 |
2 | HG02015.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.200-895G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12577169 | |||||||
chr7:12577408 | A | G | 1 | a0005c0007t0034g0350 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.200-656A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12577408 | |||||||
chr7:12577572 | C | T | 1 | a0002c0003t0006g0234 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.200-492C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12577572 | |||||||
chr7:12577599 | C | G | 92 | a0002c0002t0001g0252 a0002c0002t0001g0258 a0002c0002t0001g0260 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.200-465C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12577599 | |||||||
chr7:12577631 | T | A | 1 | a0001c0001t0017g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.200-433T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12577631 | |||||||
chr7:12577714 | A | G | 21 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(18): Show |
21 | HG00597.hp2 HG01255.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.200-350A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12577714 | |||||||
chr7:12577728 | C | A | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.200-336C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12577728 | |||||||
chr7:12577816 | A | G | 1 | a0001c0001t0108g0204 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.200-248A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12577816 | |||||||
chr7:12577837 | C | T | 11 | a0002c0002t0002g0329 a0002c0002t0002g0330 a0002c0002t0002g0332 others(8): Show |
11 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.200-227C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12577837 | |||||||
chr7:12577855 | C | CA | 6 | a0001c0001t0020g0113 a0001c0001t0030g0115 a0001c0001t0067g0205 others(3): Show |
6 | HG00741.hp2 HG01168.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.200-195dupA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 12577855 | ||||||
chr7:12577855 | CA | C | 158 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.200-195delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 12577855 | ||||||
chr7:12577855 | CAA | C | 20 | a0002c0002t0002g0239 a0002c0002t0002g0320 a0002c0002t0002g0322 others(17): Show |
21 | HG01192.hp2 HG01243.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.200-196_200-195del others(2): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 12577855 | ||||||
chr7:12577855 | CAAA | C | 10 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(7): Show |
10 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.200-197_200-195del others(3): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 12577855 | ||||||
chr7:12577927 | C | G | 83 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0091 others(80): Show |
86 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.200-137C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12577927 | |||||||
chr7:12577969 | T | C | 1 | a0001c0001t0138g0080 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.200-95T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 1/15 | chr7 | 12577969 | |||||||
chr7:12578229 | C | T | 7 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(4): Show |
7 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.354+11C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12578229 | |||||||
chr7:12578388 | G | A | 19 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(16): Show |
19 | HG02027.hp2 HG02135.hp1 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.354+170G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12578388 | |||||||
chr7:12578508 | G | T | 200 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.354+290G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12578508 | |||||||
chr7:12578562 | G | C | 1 | a0001c0001t0173g0081 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.354+344G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12578562 | |||||||
chr7:12578783 | C | G | 10 | a0001c0001t0004g0108 a0001c0001t0012g0106 a0001c0001t0018g0110 others(7): Show |
10 | HG00438.hp1 HG02004.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.354+565C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12578783 | |||||||
chr7:12578785 | C | T | 3 | a0009c0012t0080g0283 a0009c0012t0082g0284 a0009c0012t0085g0282 |
3 | HG02257.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.354+567C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12578785 | |||||||
chr7:12578793 | C | T | 1 | a0004c0005t0019g0177 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.354+575C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12578793 | |||||||
chr7:12578832 | G | T | 1 | a0006c0006t0018g0176 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.354+614G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12578832 | |||||||
chr7:12578891 | G | A | 1 | a0001c0001t0127g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.354+673G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12578891 | |||||||
chr7:12578909 | G | GTTTTTGT others(27): Show |
1 | a0001c0001t0016g0023 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.354+696_354+697ins others(34): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(2): Show |
26 | a0002c0002t0001g0258 a0002c0002t0001g0260 a0002c0002t0001g0268 others(23): Show |
26 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.354+698_354+706dup others(9): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(3): Show |
4 | a0002c0002t0001g0252 a0002c0002t0001g0276 a0002c0002t0007g0275 others(1): Show |
4 | HG00423.hp2 HG00597.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+697_354+706dup others(10): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(4): Show |
1 | a0002c0002t0113g0277 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.354+696_354+706dup others(11): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(9): Show |
1 | a0002c0002t0007g0288 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.354+703_354+704ins others(16): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(8): Show |
17 | a0001c0001t0052g0343 a0001c0001t0053g0344 a0001c0001t0054g0345 others(14): Show |
18 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.354+692_354+706dup others(15): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(9): Show |
25 | a0001c0001t0037g0012 a0001c0001t0050g0349 a0001c0001t0051g0347 others(22): Show |
25 | HG00741.hp1 HG01175.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(16): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(10): Show |
11 | a0002c0002t0158g0298 a0002c0003t0008g0250 a0002c0003t0057g0360 others(8): Show |
11 | HG00597.hp2 HG00673.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(17): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(11): Show |
1 | a0008c0009t0160g0243 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.354+706_354+707ins others(18): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(25): Show |
1 | a0002c0002t0114g0289 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.354+706_354+707ins others(32): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(26): Show |
2 | a0002c0002t0004g0290 a0002c0002t0026g0291 |
2 | HG01346.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.354+706_354+707ins others(33): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(27): Show |
3 | a0002c0002t0003g0294 a0002c0002t0091g0292 a0002c0002t0169g0293 |
3 | HG01123.hp1 HG01515.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.354+706_354+707ins others(34): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(16): Show |
3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0002c0003t0006g0236 |
3 | HG02165.hp2 HG03225.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.354+706_354+707ins others(23): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(24): Show |
1 | a0001c0001t0172g0024 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.354+706_354+707ins others(31): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(25): Show |
1 | a0001c0001t0009g0025 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.354+706_354+707ins others(32): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(17): Show |
1 | a0002c0014t0184g0059 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.354+706_354+707ins others(24): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(18): Show |
4 | a0002c0003t0017g0231 a0002c0003t0143g0232 a0002c0014t0006g0060 others(1): Show |
4 | HG02622.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(25): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(19): Show |
6 | a0002c0002t0020g0244 a0002c0002t0180g0245 a0002c0003t0006g0234 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(26): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(20): Show |
4 | a0002c0002t0002g0247 a0002c0002t0020g0246 a0002c0003t0089g0235 others(1): Show |
4 | HG02630.hp1 HG03516.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(27): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(22): Show |
9 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0009g0056 others(6): Show |
9 | HG00099.hp1 HG01167.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(29): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(23): Show |
11 | a0001c0001t0003g0054 a0001c0001t0006g0016 a0001c0001t0007g0051 others(8): Show |
11 | HG00408.hp1 HG01496.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(30): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(24): Show |
13 | a0001c0001t0001g0029 a0001c0001t0013g0020 a0001c0001t0014g0021 others(10): Show |
13 | HG00642.hp1 HG00642.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(31): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(25): Show |
1 | a0001c0001t0117g0030 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.354+706_354+707ins others(32): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(26): Show |
9 | a0001c0001t0027g0042 a0002c0002t0001g0304 a0002c0002t0002g0301 others(6): Show |
9 | HG00140.hp1 HG01169.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(33): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(27): Show |
14 | a0002c0002t0001g0308 a0002c0002t0001g0311 a0002c0002t0002g0239 others(11): Show |
14 | HG00323.hp1 HG01346.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(34): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(28): Show |
10 | a0001c0001t0009g0031 a0002c0002t0010g0317 a0002c0002t0012g0278 others(7): Show |
10 | HG01243.hp1 HG02080.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(35): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(29): Show |
4 | a0002c0002t0157g0328 a0009c0012t0080g0283 a0009c0012t0082g0284 others(1): Show |
4 | HG02257.hp2 HG03017.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(36): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(30): Show |
1 | a0002c0002t0079g0280 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.354+706_354+707ins others(37): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(31): Show |
4 | a0001c0001t0119g0032 a0002c0002t0002g0329 a0002c0002t0002g0330 others(1): Show |
4 | HG03195.hp2 HG03492.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+706_354+707ins others(38): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(32): Show |
2 | a0002c0002t0002g0332 a0002c0002t0167g0331 |
2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.354+706_354+707ins others(39): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(34): Show |
2 | a0001c0001t0011g0034 a0001c0001t0035g0033 |
2 | HG02135.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.354+706_354+707ins others(41): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(35): Show |
3 | a0001c0001t0003g0037 a0001c0001t0073g0036 a0001c0001t0163g0035 |
3 | HG03831.hp2 NA18943.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.354+706_354+707ins others(42): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(36): Show |
1 | a0019c0015t0013g0038 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.354+706_354+707ins others(43): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12578909 | G | GTTTTTTT others(37): Show |
2 | a0001c0001t0095g0039 a0002c0002t0182g0333 |
2 | HG01168.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.354+706_354+707ins others(44): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12578909 | ||||||
chr7:12579059 | G | A | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.354+841G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579059 | |||||||
chr7:12579139 | T | C | 51 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(48): Show |
53 | HG00597.hp2 HG00738.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.354+921T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579139 | |||||||
chr7:12579170 | G | A | 3 | a0002c0003t0008g0249 a0002c0003t0008g0250 a0002c0003t0022g0248 |
3 | HG01256.hp1 HG01261.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.354+952G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579170 | |||||||
chr7:12579266 | A | G | 7 | a0001c0001t0001g0029 a0001c0001t0009g0025 a0001c0001t0009g0031 others(4): Show |
7 | HG02027.hp2 NA18949.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.354+1048A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579266 | |||||||
chr7:12579299 | T | G | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.354+1081T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579299 | |||||||
chr7:12579365 | C | T | 11 | a0002c0003t0006g0234 a0002c0003t0006g0236 a0002c0003t0017g0231 others(8): Show |
12 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.354+1147C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579365 | |||||||
chr7:12579392 | G | A | 2 | a0001c0001t0020g0113 a0001c0001t0136g0117 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.354+1174G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579392 | |||||||
chr7:12579432 | A | T | 13 | a0002c0003t0006g0337 a0002c0003t0008g0249 a0002c0003t0008g0250 others(10): Show |
14 | HG01256.hp1 HG01261.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.354+1214A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579432 | |||||||
chr7:12579436 | A | G | 1 | a0002c0002t0016g0274 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.354+1218A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579436 | |||||||
chr7:12579476 | C | A | 9 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.354+1258C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579476 | |||||||
chr7:12579594 | G | T | 2 | a0001c0001t0022g0174 a0001c0001t0022g0175 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.354+1376G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579594 | |||||||
chr7:12579670 | C | T | 7 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(4): Show |
7 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.355-1390C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579670 | |||||||
chr7:12579737 | G | A | 16 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(13): Show |
16 | HG00597.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.355-1323G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579737 | |||||||
chr7:12579743 | C | G | 96 | a0002c0002t0001g0252 a0002c0002t0001g0258 a0002c0002t0001g0260 others(93): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.355-1317C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579743 | |||||||
chr7:12579845 | C | A | 1 | a0002c0002t0003g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.355-1215C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12579845 | |||||||
chr7:12580028 | TA | T | 4 | a0002c0002t0004g0273 a0002c0002t0005g0270 a0002c0002t0008g0271 others(1): Show |
4 | HG01928.hp1 HG01943.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-1031delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12580028 | |||||||
chr7:12580031 | T | A | 63 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(60): Show |
64 | HG00099.hp1 HG00408.hp1 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.355-1029T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12580031 | |||||||
chr7:12580100 | C | A | 2 | a0002c0003t0061g0359 a0002c0003t0062g0355 |
2 | NA18944.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.355-960C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12580100 | |||||||
chr7:12580115 | A | G | 203 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(200): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.355-945A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12580115 | |||||||
chr7:12580310 | GATC | G | 41 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(38): Show |
42 | HG00597.hp2 HG00738.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.355-747_355-745del others(3): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 12580310 | ||||||
chr7:12580376 | T | C | 3 | a0001c0001t0003g0206 a0001c0001t0005g0208 a0001c0001t0021g0207 |
3 | NA18960.hp1 NA19000.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.355-684T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12580376 | |||||||
chr7:12580575 | C | T | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.355-485C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12580575 | |||||||
chr7:12580718 | C | G | 1 | a0007c0008t0009g0172 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.355-342C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12580718 | |||||||
chr7:12580728 | T | A | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.355-332T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12580728 | |||||||
chr7:12580753 | C | T | 146 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(143): Show |
146 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.355-307C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12580753 | |||||||
chr7:12580825 | C | A | 1 | a0005c0007t0034g0350 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355-235C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12580825 | |||||||
chr7:12581046 | C | T | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.355-14C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 2/15 | chr7 | 12581046 | |||||||
chr7:12581561 | G | T | 1 | a0001c0001t0173g0081 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.516+340G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12581561 | |||||||
chr7:12581602 | A | G | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+381A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12581602 | |||||||
chr7:12581744 | T | C | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+523T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12581744 | |||||||
chr7:12581819 | T | C | 3 | a0002c0002t0001g0258 a0002c0002t0023g0254 a0002c0002t0084g0259 |
3 | NA18952.hp1 NA18959.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.516+598T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12581819 | |||||||
chr7:12581907 | T | C | 1 | a0002c0002t0113g0277 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.516+686T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12581907 | |||||||
chr7:12581912 | T | A | 1 | a0001c0001t0025g0218 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.516+691T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12581912 | |||||||
chr7:12582021 | T | C | 12 | a0002c0003t0006g0337 a0002c0003t0008g0249 a0002c0003t0008g0250 others(9): Show |
13 | HG01256.hp1 HG01261.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.516+800T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12582021 | |||||||
chr7:12582032 | C | G | 4 | a0008c0009t0006g0242 a0008c0009t0110g0240 a0008c0009t0159g0241 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+811C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12582032 | |||||||
chr7:12582089 | C | T | 2 | a0001c0001t0002g0170 a0001c0001t0176g0171 |
2 | HG00408.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.516+868C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12582089 | |||||||
chr7:12582207 | T | G | 202 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(199): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.516+986T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12582207 | |||||||
chr7:12582455 | G | A | 2 | a0001c0001t0037g0012 a0001c0001t0166g0011 |
2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.516+1234G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12582455 | |||||||
chr7:12582576 | G | T | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.516+1355G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12582576 | |||||||
chr7:12582762 | A | G | 1 | a0001c0001t0037g0012 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.516+1541A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12582762 | |||||||
chr7:12582991 | T | C | 1 | a0001c0001t0014g0112 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.516+1770T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12582991 | |||||||
chr7:12583043 | C | G | 46 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(43): Show |
47 | HG00597.hp2 HG00738.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.516+1822C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12583043 | |||||||
chr7:12583051 | GA | G | 9 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+1833delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12583051 | ||||||
chr7:12583114 | T | C | 1 | a0005c0007t0034g0350 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.516+1893T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12583114 | |||||||
chr7:12583146 | T | A | 25 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(22): Show |
25 | HG00597.hp2 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.516+1925T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12583146 | |||||||
chr7:12583179 | A | G | 2 | a0001c0001t0003g0119 a0010c0011t0135g0353 |
2 | HG02976.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.516+1958A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12583179 | |||||||
chr7:12583249 | C | G | 11 | a0002c0003t0006g0234 a0002c0003t0006g0236 a0002c0003t0017g0231 others(8): Show |
12 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+2028C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12583249 | |||||||
chr7:12583845 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.516+2624T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12583845 | |||||||
chr7:12583995 | A | G | 92 | a0001c0001t0003g0119 a0002c0002t0001g0252 a0002c0002t0001g0258 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.516+2774A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12583995 | |||||||
chr7:12584062 | A | G | 12 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(9): Show |
12 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.516+2841A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12584062 | |||||||
chr7:12584253 | A | G | 3 | a0008c0009t0006g0242 a0008c0009t0159g0241 a0008c0009t0160g0243 |
3 | HG02809.hp1 HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.516+3032A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12584253 | |||||||
chr7:12584396 | A | C | 3 | a0002c0002t0041g0325 a0002c0002t0041g0326 a0002c0002t0182g0333 |
3 | HG00642.hp1 HG01168.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.516+3175A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12584396 | |||||||
chr7:12584420 | A | G | 9 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+3199A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12584420 | |||||||
chr7:12584596 | A | T | 1 | a0001c0001t0002g0169 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.516+3375A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12584596 | |||||||
chr7:12584675 | G | A | 2 | a0002c0002t0007g0275 a0002c0002t0098g0253 |
2 | HG00423.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.516+3454G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12584675 | |||||||
chr7:12584677 | C | T | 203 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(200): Show |
205 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.516+3456C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12584677 | |||||||
chr7:12584702 | T | C | 3 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0002t0020g0246 |
3 | HG02280.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.516+3481T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12584702 | |||||||
chr7:12584731 | T | C | 24 | a0001c0001t0051g0347 a0001c0001t0052g0343 a0001c0001t0053g0344 others(21): Show |
24 | HG00597.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.516+3510T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12584731 | |||||||
chr7:12584849 | A | G | 1 | a0002c0002t0069g0269 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.516+3628A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12584849 | |||||||
chr7:12585002 | A | G | 2 | a0001c0001t0021g0010 a0001c0001t0117g0030 |
2 | NA18949.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.516+3781A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12585002 | |||||||
chr7:12585018 | C | T | 12 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(9): Show |
12 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.516+3797C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12585018 | |||||||
chr7:12585218 | G | C | 206 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(203): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.516+3997G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12585218 | |||||||
chr7:12585230 | G | C | 1 | a0002c0003t0002g0255 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.516+4009G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12585230 | |||||||
chr7:12585311 | C | T | 5 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0002t0020g0246 others(2): Show |
5 | HG02280.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+4090C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12585311 | |||||||
chr7:12585584 | A | G | 1 | a0002c0002t0113g0277 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.516+4363A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12585584 | |||||||
chr7:12585722 | A | G | 1 | a0002c0002t0079g0280 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.516+4501A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12585722 | |||||||
chr7:12585790 | G | A | 1 | a0002c0003t0059g0362 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.516+4569G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12585790 | |||||||
chr7:12585854 | C | T | 7 | a0002c0003t0006g0234 a0002c0003t0017g0231 a0002c0003t0017g0233 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.516+4633C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12585854 | |||||||
chr7:12585916 | C | T | 1 | a0001c0001t0176g0171 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.516+4695C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12585916 | |||||||
chr7:12585918 | C | T | 11 | a0002c0003t0006g0234 a0002c0003t0006g0236 a0002c0003t0017g0231 others(8): Show |
12 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+4697C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12585918 | |||||||
chr7:12586077 | A | G | 1 | a0001c0001t0017g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.516+4856A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12586077 | |||||||
chr7:12586172 | A | C | 1 | a0016c0016t0148g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.516+4951A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12586172 | |||||||
chr7:12586203 | C | G | 352 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(349): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.516+4982C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12586203 | |||||||
chr7:12586215 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0003g0206 a0001c0001t0004g0213 others(5): Show |
8 | HG01361.hp1 HG01928.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.516+4994A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12586215 | |||||||
chr7:12586267 | G | A | 1 | a0002c0002t0156g0306 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.516+5046G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12586267 | |||||||
chr7:12586513 | C | T | 5 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0133g0198 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+5292C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12586513 | |||||||
chr7:12586533 | A | G | 1 | a0002c0002t0031g0285 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.516+5312A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12586533 | |||||||
chr7:12586665 | C | T | 1 | a0002c0002t0008g0058 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.516+5444C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12586665 | |||||||
chr7:12586676 | A | G | 57 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(54): Show |
59 | HG00597.hp2 HG00738.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.516+5455A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12586676 | |||||||
chr7:12586825 | C | T | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+5604C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12586825 | |||||||
chr7:12586920 | T | G | 1 | a0002c0003t0006g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.516+5699T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12586920 | |||||||
chr7:12587008 | C | T | 1 | a0002c0003t0142g0341 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.516+5787C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587008 | |||||||
chr7:12587013 | G | C | 207 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(204): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.516+5792G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587013 | |||||||
chr7:12587106 | G | A | 24 | a0002c0003t0006g0063 a0002c0003t0006g0337 a0002c0003t0008g0249 others(21): Show |
25 | HG01256.hp1 HG01261.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.516+5885G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587106 | |||||||
chr7:12587294 | C | T | 5 | a0002c0003t0006g0337 a0005c0007t0006g0335 a0005c0007t0047g0338 others(2): Show |
6 | HG02145.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.516+6073C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587294 | |||||||
chr7:12587380 | T | C | 90 | a0001c0001t0003g0119 a0002c0002t0001g0252 a0002c0002t0001g0258 others(87): Show |
90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.516+6159T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587380 | |||||||
chr7:12587384 | G | A | 4 | a0001c0001t0003g0002 a0001c0001t0003g0083 a0001c0001t0003g0084 others(1): Show |
5 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+6163G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587384 | |||||||
chr7:12587385 | T | A | 9 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+6164T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587385 | |||||||
chr7:12587388 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.516+6167G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587388 | |||||||
chr7:12587457 | C | T | 1 | a0002c0002t0005g0319 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.516+6236C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587457 | |||||||
chr7:12587477 | C | A | 195 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(192): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.516+6256C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587477 | |||||||
chr7:12587594 | CT | C | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+6374delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587594 | |||||||
chr7:12587620 | A | G | 195 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(192): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.516+6399A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587620 | |||||||
chr7:12587634 | C | T | 1 | a0002c0003t0089g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.516+6413C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587634 | |||||||
chr7:12587651 | C | G | 1 | a0001c0001t0010g0167 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.516+6430C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587651 | |||||||
chr7:12587671 | G | C | 1 | a0002c0002t0158g0298 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.516+6450G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587671 | |||||||
chr7:12587767 | T | C | 4 | a0008c0009t0006g0242 a0008c0009t0110g0240 a0008c0009t0159g0241 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+6546T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587767 | |||||||
chr7:12587808 | A | C | 11 | a0002c0003t0006g0234 a0002c0003t0006g0236 a0002c0003t0017g0231 others(8): Show |
12 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+6587A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587808 | |||||||
chr7:12587872 | T | C | 9 | a0002c0003t0006g0337 a0005c0007t0006g0335 a0005c0007t0047g0338 others(6): Show |
10 | HG02145.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.516+6651T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587872 | |||||||
chr7:12587917 | G | A | 3 | a0002c0003t0089g0235 a0002c0003t0134g0237 a0011c0013t0014g0238 |
3 | HG02630.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.516+6696G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587917 | |||||||
chr7:12587935 | A | G | 207 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(204): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.516+6714A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587935 | |||||||
chr7:12587959 | C | T | 5 | a0001c0001t0003g0119 a0002c0002t0004g0273 a0002c0002t0005g0270 others(2): Show |
5 | HG01928.hp1 HG01943.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+6738C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12587959 | |||||||
chr7:12588194 | A | G | 1 | a0002c0002t0001g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.516+6973A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588194 | |||||||
chr7:12588273 | G | A | 13 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(10): Show |
13 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.516+7052G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588273 | |||||||
chr7:12588345 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0002g0169 |
2 | HG01099.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.516+7124T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588345 | |||||||
chr7:12588364 | G | C | 1 | a0002c0002t0158g0298 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.516+7143G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588364 | |||||||
chr7:12588395 | G | A | 1 | a0008c0009t0110g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.516+7174G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588395 | |||||||
chr7:12588492 | G | T | 3 | a0001c0001t0121g0201 a0001c0001t0185g0200 a0004c0005t0014g0202 |
3 | HG02572.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.516+7271G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588492 | |||||||
chr7:12588625 | G | A | 1 | a0001c0001t0101g0122 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.516+7404G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588625 | |||||||
chr7:12588628 | A | C | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.516+7407A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588628 | |||||||
chr7:12588744 | T | C | 183 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.516+7523T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588744 | |||||||
chr7:12588804 | T | TG | 4 | a0002c0002t0020g0246 a0002c0002t0079g0280 a0002c0002t0129g0007 others(1): Show |
4 | HG01257.hp1 HG01258.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+7586dupG | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12588804 | ||||||
chr7:12588806 | GGT | G | 43 | a0002c0002t0001g0258 a0002c0002t0002g0239 a0002c0002t0002g0267 others(40): Show |
43 | HG00558.hp2 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.516+7587_516+7588d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12588806 | ||||||
chr7:12588807 | GT | G | 25 | a0002c0002t0001g0304 a0002c0002t0001g0311 a0002c0002t0002g0301 others(22): Show |
25 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.516+7587delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588807 | |||||||
chr7:12588807 | GTGGGGGG others(24): Show |
G | 4 | a0002c0003t0015g0340 a0002c0003t0015g0342 a0002c0003t0016g0339 others(1): Show |
4 | HG02109.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+7587_516+7617d others(33): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588807 | |||||||
chr7:12588808 | T | C | 2 | a0002c0002t0001g0252 a0002c0002t0175g0251 |
2 | HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.516+7587T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588808 | |||||||
chr7:12588808 | T | G | 18 | a0001c0001t0003g0119 a0002c0002t0001g0260 a0002c0002t0001g0268 others(15): Show |
18 | HG00099.hp2 HG00597.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.516+7587T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588808 | |||||||
chr7:12588808 | TG | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0101 others(70): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.516+7600delG | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12588808 | ||||||
chr7:12588821 | G | C | 1 | a0001c0001t0179g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.516+7600G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588821 | |||||||
chr7:12588821 | GT | G | 5 | a0001c0001t0051g0347 a0001c0001t0121g0201 a0002c0002t0175g0251 others(2): Show |
5 | HG01175.hp1 HG03579.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+7601delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588821 | |||||||
chr7:12588821 | GTGC | G | 5 | a0001c0001t0050g0349 a0001c0001t0185g0200 a0002c0003t0056g0358 others(2): Show |
5 | HG02523.hp1 HG02572.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+7601_516+7603d others(5): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588821 | |||||||
chr7:12588822 | T | G | 183 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.516+7601T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588822 | |||||||
chr7:12588824 | C | G | 19 | a0001c0001t0051g0347 a0001c0001t0052g0343 a0001c0001t0053g0344 others(16): Show |
20 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.516+7603C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588824 | |||||||
chr7:12588827 | G | C | 43 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(40): Show |
43 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.516+7606G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588827 | |||||||
chr7:12588829 | GC | G | 39 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(36): Show |
39 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.516+7609delC | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588829 | |||||||
chr7:12588830 | C | G | 4 | a0001c0001t0029g0019 a0001c0001t0093g0043 a0001c0001t0096g0050 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+7609C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588830 | |||||||
chr7:12588833 | GTGGGA | G | 14 | a0002c0002t0001g0276 a0002c0002t0001g0304 a0002c0002t0002g0267 others(11): Show |
14 | HG00597.hp1 HG01106.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.516+7613_516+7617d others(7): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588833 | |||||||
chr7:12588833 | GTGGGAA | G | 80 | a0001c0001t0003g0119 a0002c0002t0001g0252 a0002c0002t0001g0258 others(77): Show |
80 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.516+7613_516+7618d others(8): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588833 | |||||||
chr7:12588834 | T | C | 43 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(40): Show |
43 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.516+7613T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588834 | |||||||
chr7:12588834 | T | G | 29 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(26): Show |
30 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.516+7613T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588834 | |||||||
chr7:12588834 | TGGGAAG | T | 17 | a0001c0001t0011g0034 a0001c0001t0021g0010 a0001c0001t0037g0012 others(14): Show |
17 | HG00099.hp1 HG00597.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.516+7617_516+7622d others(8): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12588834 | ||||||
chr7:12588836 | G | C | 25 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(22): Show |
26 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.516+7615G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588836 | |||||||
chr7:12588837 | GA | G | 5 | a0002c0003t0006g0337 a0005c0007t0006g0335 a0005c0007t0047g0338 others(2): Show |
6 | HG02145.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.516+7618delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12588837 | ||||||
chr7:12588837 | GAA | G | 45 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(42): Show |
45 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.516+7617_516+7618d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588837 | |||||||
chr7:12588838 | A | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0088 others(194): Show |
202 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.516+7617A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588838 | |||||||
chr7:12588839 | A | G | 48 | a0001c0001t0050g0349 a0001c0001t0051g0347 a0001c0001t0052g0343 others(45): Show |
50 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.516+7618A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588839 | |||||||
chr7:12588840 | G | T | 70 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(67): Show |
71 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.516+7619G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588840 | |||||||
chr7:12588845 | A | C | 3 | a0008c0009t0006g0242 a0008c0009t0159g0241 a0008c0009t0160g0243 |
3 | HG02809.hp1 HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.516+7624A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588845 | |||||||
chr7:12588910 | G | A | 1 | a0001c0001t0005g0212 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.516+7689G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588910 | |||||||
chr7:12588949 | T | C | 13 | a0002c0002t0001g0268 a0002c0003t0006g0063 a0002c0003t0014g0069 others(10): Show |
13 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.516+7728T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588949 | |||||||
chr7:12588952 | G | C | 5 | a0001c0001t0017g0220 a0002c0003t0014g0069 a0002c0003t0037g0071 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+7731G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588952 | |||||||
chr7:12588952 | G | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0002g0145 others(9): Show |
12 | HG00735.hp2 HG01361.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.516+7731G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588952 | |||||||
chr7:12588953 | G | C | 1 | a0001c0001t0099g0103 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.516+7732G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588953 | |||||||
chr7:12588957 | A | G | 1 | a0002c0002t0031g0285 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.516+7736A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12588957 | |||||||
chr7:12589135 | G | T | 9 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+7914G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589135 | |||||||
chr7:12589182 | G | A | 33 | a0001c0001t0001g0079 a0001c0001t0001g0124 a0001c0001t0001g0125 others(30): Show |
34 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.516+7961G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589182 | |||||||
chr7:12589215 | C | CT | 33 | a0001c0001t0002g0170 a0001c0001t0003g0037 a0001c0001t0003g0206 others(30): Show |
34 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.516+8013dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12589215 | ||||||
chr7:12589215 | CT | C | 14 | a0002c0003t0006g0234 a0002c0003t0006g0236 a0002c0003t0017g0231 others(11): Show |
15 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.516+8013delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12589215 | ||||||
chr7:12589309 | C | T | 3 | a0001c0001t0004g0108 a0001c0001t0086g0107 a0001c0001t0125g0111 |
3 | HG02004.hp1 HG02300.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.516+8088C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589309 | |||||||
chr7:12589368 | T | C | 93 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(90): Show |
94 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.516+8147T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589368 | |||||||
chr7:12589381 | G | A | 1 | a0002c0003t0016g0339 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.516+8160G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589381 | |||||||
chr7:12589406 | G | C | 1 | a0001c0001t0050g0349 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.516+8185G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589406 | |||||||
chr7:12589416 | G | A | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.516+8195G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589416 | |||||||
chr7:12589664 | T | G | 2 | a0001c0001t0045g0211 a0001c0001t0122g0210 |
2 | NA18947.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.516+8443T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589664 | |||||||
chr7:12589672 | C | T | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+8451C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589672 | |||||||
chr7:12589784 | G | C | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.516+8563G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589784 | |||||||
chr7:12589853 | G | A | 16 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0003g0054 others(13): Show |
16 | HG00099.hp1 HG00408.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.516+8632G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589853 | |||||||
chr7:12589872 | T | C | 2 | a0001c0001t0045g0211 a0001c0001t0122g0210 |
2 | NA18947.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.516+8651T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589872 | |||||||
chr7:12589943 | A | C | 2 | a0002c0010t0068g0265 a0002c0010t0128g0266 |
2 | HG01106.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.516+8722A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589943 | |||||||
chr7:12589995 | AT | A | 99 | a0001c0001t0003g0119 a0002c0002t0001g0252 a0002c0002t0001g0258 others(96): Show |
99 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.516+8777delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12589995 | ||||||
chr7:12589999 | G | A | 11 | a0002c0003t0006g0234 a0002c0003t0006g0236 a0002c0003t0017g0231 others(8): Show |
12 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+8778G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12589999 | |||||||
chr7:12590053 | TGGATGCC others(2): Show |
T | 4 | a0001c0001t0001g0101 a0001c0001t0024g0099 a0001c0001t0115g0100 others(1): Show |
4 | HG02040.hp2 HG02155.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+8835_516+8843d others(11): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12590053 | ||||||
chr7:12590133 | G | T | 62 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(59): Show |
62 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.516+8912G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590133 | |||||||
chr7:12590144 | G | C | 207 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(204): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.516+8923G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590144 | |||||||
chr7:12590162 | A | G | 4 | a0002c0003t0015g0340 a0002c0003t0015g0342 a0002c0003t0016g0339 others(1): Show |
4 | HG02109.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+8941A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590162 | |||||||
chr7:12590229 | A | G | 51 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(48): Show |
51 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.516+9008A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590229 | |||||||
chr7:12590355 | G | A | 9 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+9134G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590355 | |||||||
chr7:12590397 | A | G | 1 | a0009c0012t0082g0284 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.516+9176A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590397 | |||||||
chr7:12590468 | C | T | 1 | a0002c0003t0063g0357 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.516+9247C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590468 | |||||||
chr7:12590477 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0010c0011t0135g0353 |
3 | HG02165.hp2 HG02976.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.516+9256A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590477 | |||||||
chr7:12590533 | C | T | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.516+9312C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590533 | |||||||
chr7:12590558 | G | A | 10 | a0001c0001t0004g0108 a0001c0001t0012g0106 a0001c0001t0018g0110 others(7): Show |
10 | HG00438.hp1 HG02004.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.516+9337G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590558 | |||||||
chr7:12590577 | G | C | 253 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(250): Show |
257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.516+9356G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590577 | |||||||
chr7:12590602 | G | A | 1 | a0002c0010t0001g0261 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.516+9381G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590602 | |||||||
chr7:12590742 | C | T | 9 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+9521C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590742 | |||||||
chr7:12590800 | G | A | 1 | a0001c0001t0050g0349 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.516+9579G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590800 | |||||||
chr7:12590807 | A | G | 1 | a0001c0001t0019g0230 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.516+9586A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590807 | |||||||
chr7:12590824 | C | T | 3 | a0008c0009t0006g0242 a0008c0009t0159g0241 a0008c0009t0160g0243 |
3 | HG02809.hp1 HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.516+9603C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12590824 | |||||||
chr7:12591205 | G | A | 4 | a0008c0009t0006g0242 a0008c0009t0110g0240 a0008c0009t0159g0241 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+9984G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12591205 | |||||||
chr7:12591256 | G | C | 1 | a0002c0002t0158g0298 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.516+10035G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12591256 | |||||||
chr7:12591295 | T | C | 1 | a0002c0002t0126g0315 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.516+10074T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12591295 | |||||||
chr7:12591560 | T | C | 1 | a0001c0001t0119g0032 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.516+10339T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12591560 | |||||||
chr7:12591571 | C | T | 5 | a0002c0003t0006g0337 a0005c0007t0006g0335 a0005c0007t0047g0338 others(2): Show |
6 | HG02145.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.516+10350C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12591571 | |||||||
chr7:12591610 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.516+10389G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12591610 | |||||||
chr7:12591676 | G | A | 5 | a0007c0008t0003g0154 a0007c0008t0009g0172 a0007c0008t0039g0155 others(2): Show |
5 | NA18951.hp2 NA18966.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+10455G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12591676 | |||||||
chr7:12591681 | G | T | 1 | a0005c0007t0034g0350 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.516+10460G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12591681 | |||||||
chr7:12591686 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0002g0145 |
2 | HG00735.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.516+10465G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12591686 | |||||||
chr7:12592021 | A | G | 351 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(348): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.516+10800A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592021 | |||||||
chr7:12592137 | C | A | 5 | a0001c0001t0052g0343 a0001c0001t0053g0344 a0001c0001t0054g0345 others(2): Show |
5 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+10916C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592137 | |||||||
chr7:12592295 | C | T | 219 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(216): Show |
224 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.516+11074C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592295 | |||||||
chr7:12592357 | A | T | 1 | a0002c0002t0150g0318 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.516+11136A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592357 | |||||||
chr7:12592393 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.516+11172G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592393 | |||||||
chr7:12592443 | T | C | 4 | a0002c0003t0015g0340 a0002c0003t0015g0342 a0002c0003t0016g0339 others(1): Show |
4 | HG02109.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+11222T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592443 | |||||||
chr7:12592459 | A | G | 344 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(341): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.516+11238A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592459 | |||||||
chr7:12592460 | T | C | 172 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(169): Show |
174 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.516+11239T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592460 | |||||||
chr7:12592479 | C | G | 1 | a0001c0001t0003g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.516+11258C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592479 | |||||||
chr7:12592603 | C | G | 1 | a0003c0004t0004g0133 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.516+11382C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592603 | |||||||
chr7:12592697 | G | C | 1 | a0001c0001t0108g0204 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.516+11476G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592697 | |||||||
chr7:12592726 | G | C | 1 | a0005c0007t0034g0350 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.516+11505G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592726 | |||||||
chr7:12592754 | C | T | 1 | a0006c0006t0139g0132 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.516+11533C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592754 | |||||||
chr7:12592841 | G | A | 1 | a0001c0001t0032g0082 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.516+11620G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592841 | |||||||
chr7:12592929 | G | A | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.517-11585G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12592929 | |||||||
chr7:12593142 | G | A | 98 | a0001c0001t0003g0119 a0001c0001t0050g0349 a0002c0002t0001g0252 others(95): Show |
98 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.517-11372G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593142 | |||||||
chr7:12593149 | G | C | 335 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(332): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.517-11365G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593149 | |||||||
chr7:12593293 | C | T | 3 | a0002c0002t0002g0329 a0002c0002t0002g0330 a0002c0002t0002g0332 |
3 | HG03491.hp2 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.517-11221C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593293 | |||||||
chr7:12593387 | CT | C | 7 | a0002c0003t0006g0234 a0002c0003t0017g0231 a0002c0003t0017g0233 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.517-11122delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12593387 | ||||||
chr7:12593404 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.517-11110G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593404 | |||||||
chr7:12593433 | C | T | 335 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(332): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.517-11081C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593433 | |||||||
chr7:12593463 | G | A | 9 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-11051G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593463 | |||||||
chr7:12593520 | A | G | 3 | a0001c0001t0011g0153 a0001c0001t0024g0131 a0001c0001t0044g0130 |
3 | NA18951.hp1 NA19068.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.517-10994A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593520 | |||||||
chr7:12593535 | T | A | 7 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(4): Show |
7 | HG00597.hp2 HG02523.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-10979T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593535 | |||||||
chr7:12593682 | G | A | 1 | a0001c0001t0116g0136 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.517-10832G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593682 | |||||||
chr7:12593752 | G | T | 334 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(331): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.517-10762G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593752 | |||||||
chr7:12593764 | G | A | 5 | a0001c0001t0052g0343 a0001c0001t0053g0344 a0001c0001t0054g0345 others(2): Show |
5 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-10750G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593764 | |||||||
chr7:12593871 | T | C | 1 | a0001c0001t0149g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.517-10643T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593871 | |||||||
chr7:12593889 | G | A | 6 | a0001c0001t0001g0088 a0001c0001t0002g0087 a0001c0001t0005g0094 others(3): Show |
6 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-10625G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12593889 | |||||||
chr7:12594127 | G | T | 4 | a0002c0003t0015g0340 a0002c0003t0015g0342 a0002c0003t0016g0339 others(1): Show |
4 | HG02109.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-10387G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594127 | |||||||
chr7:12594136 | G | A | 6 | a0001c0001t0050g0349 a0001c0001t0052g0343 a0001c0001t0053g0344 others(3): Show |
6 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-10378G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594136 | |||||||
chr7:12594206 | G | A | 3 | a0002c0002t0012g0303 a0002c0002t0155g0307 a0002c0002t0168g0316 |
3 | NA18939.hp2 NA19002.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.517-10308G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594206 | |||||||
chr7:12594220 | C | T | 1 | a0002c0003t0022g0248 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.517-10294C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594220 | |||||||
chr7:12594283 | G | A | 5 | a0001c0001t0052g0343 a0001c0001t0053g0344 a0001c0001t0054g0345 others(2): Show |
5 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-10231G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594283 | |||||||
chr7:12594286 | G | C | 4 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0002t0020g0246 others(1): Show |
4 | HG02280.hp2 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-10228G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594286 | |||||||
chr7:12594306 | C | T | 2 | a0001c0001t0022g0174 a0001c0001t0022g0175 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.517-10208C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594306 | |||||||
chr7:12594330 | C | T | 88 | a0001c0001t0003g0119 a0002c0002t0001g0252 a0002c0002t0001g0258 others(85): Show |
88 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.517-10184C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594330 | |||||||
chr7:12594411 | G | A | 2 | a0009c0012t0080g0283 a0009c0012t0082g0284 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.517-10103G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594411 | |||||||
chr7:12594524 | G | A | 1 | a0001c0001t0093g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.517-9990G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594524 | |||||||
chr7:12594618 | G | A | 1 | a0002c0002t0001g0308 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.517-9896G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594618 | |||||||
chr7:12594831 | C | T | 6 | a0006c0006t0007g0151 a0006c0006t0011g0152 a0006c0006t0018g0176 others(3): Show |
6 | NA18940.hp1 NA18945.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-9683C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594831 | |||||||
chr7:12594853 | G | A | 5 | a0001c0001t0052g0343 a0001c0001t0053g0344 a0001c0001t0054g0345 others(2): Show |
5 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-9661G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12594853 | |||||||
chr7:12595071 | G | A | 12 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.517-9443G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12595071 | |||||||
chr7:12595075 | G | A | 1 | a0001c0001t0154g0137 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.517-9439G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12595075 | |||||||
chr7:12595207 | C | T | 9 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-9307C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12595207 | |||||||
chr7:12595294 | A | T | 1 | a0002c0002t0016g0274 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.517-9220A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12595294 | |||||||
chr7:12595313 | A | G | 9 | a0002c0003t0056g0358 a0002c0003t0057g0360 a0002c0003t0058g0361 others(6): Show |
9 | HG00597.hp2 HG01255.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-9201A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12595313 | |||||||
chr7:12595327 | G | A | 13 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(10): Show |
13 | HG01109.hp2 HG02280.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.517-9187G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12595327 | |||||||
chr7:12595499 | T | A | 1 | a0002c0002t0002g0320 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.517-9015T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12595499 | |||||||
chr7:12595564 | C | A | 3 | a0008c0009t0006g0242 a0008c0009t0159g0241 a0008c0009t0160g0243 |
3 | HG02809.hp1 HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.517-8950C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12595564 | |||||||
chr7:12595609 | G | GGAAAGAC others(194): Show |
1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517-8891_517-8890i others(203): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12595609 | ||||||
chr7:12595628 | T | C | 1 | a0002c0003t0059g0362 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.517-8886T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12595628 | |||||||
chr7:12595750 | T | A | 2 | a0002c0002t0041g0325 a0002c0002t0041g0326 |
2 | HG00642.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.517-8764T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12595750 | |||||||
chr7:12595836 | G | A | 2 | a0004c0005t0019g0177 a0004c0005t0104g0138 |
2 | HG00738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.517-8678G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12595836 | |||||||
chr7:12595852 | C | G | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517-8662C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12595852 | |||||||
chr7:12596338 | T | G | 9 | a0002c0003t0006g0063 a0002c0003t0014g0069 a0002c0003t0015g0065 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.517-8176T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12596338 | |||||||
chr7:12596360 | AAGTGCAA others(49): Show |
A | 1 | a0005c0007t0034g0350 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.517-8146_517-8091d others(58): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12596360 | ||||||
chr7:12596382 | C | T | 1 | a0001c0001t0124g0185 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.517-8132C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12596382 | |||||||
chr7:12596401 | T | C | 352 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(349): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.517-8113T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12596401 | |||||||
chr7:12596416 | T | C | 1 | a0011c0013t0014g0238 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.517-8098T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12596416 | |||||||
chr7:12596470 | A | T | 12 | a0001c0001t0133g0198 a0001c0001t0141g0199 a0002c0002t0002g0247 others(9): Show |
13 | HG02145.hp1 HG02280.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.517-8044A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12596470 | |||||||
chr7:12596494 | T | C | 1 | a0002c0002t0007g0275 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.517-8020T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12596494 | |||||||
chr7:12596576 | A | G | 1 | a0002c0002t0007g0288 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.517-7938A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12596576 | |||||||
chr7:12596592 | A | G | 6 | a0001c0001t0050g0349 a0002c0003t0006g0236 a0002c0003t0089g0235 others(3): Show |
6 | HG02258.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-7922A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12596592 | |||||||
chr7:12596670 | A | G | 1 | a0001c0001t0024g0098 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.517-7844A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12596670 | |||||||
chr7:12596686 | CT | C | 337 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(334): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.517-7816delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12596686 | ||||||
chr7:12596759 | C | T | 335 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(332): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.517-7755C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12596759 | |||||||
chr7:12596798 | G | A | 1 | a0003c0004t0004g0001 | 3 | NA18965.hp1 NA18982.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.517-7716G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12596798 | |||||||
chr7:12597071 | T | C | 1 | a0002c0003t0015g0342 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.517-7443T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12597071 | |||||||
chr7:12597370 | C | T | 2 | a0001c0001t0050g0349 a0010c0011t0135g0353 |
2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.517-7144C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12597370 | |||||||
chr7:12597476 | G | A | 1 | a0011c0013t0009g0257 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.517-7038G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12597476 | |||||||
chr7:12597486 | T | C | 34 | a0001c0001t0001g0159 a0001c0001t0003g0054 a0001c0001t0004g0108 others(31): Show |
34 | HG00544.hp2 HG01106.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.517-7028T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12597486 | |||||||
chr7:12597622 | T | C | 2 | a0001c0001t0002g0095 a0001c0001t0102g0188 |
2 | HG01891.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.517-6892T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12597622 | |||||||
chr7:12597881 | A | G | 1 | a0002c0002t0012g0303 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.517-6633A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12597881 | |||||||
chr7:12597980 | G | T | 2 | a0002c0003t0015g0065 a0002c0003t0146g0062 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.517-6534G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12597980 | |||||||
chr7:12597981 | C | T | 2 | a0002c0003t0015g0065 a0002c0003t0146g0062 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.517-6533C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12597981 | |||||||
chr7:12598072 | T | C | 1 | a0001c0001t0017g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.517-6442T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598072 | |||||||
chr7:12598123 | A | G | 1 | a0002c0002t0001g0252 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.517-6391A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598123 | |||||||
chr7:12598150 | T | G | 2 | a0001c0001t0050g0349 a0010c0011t0135g0353 |
2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.517-6364T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598150 | |||||||
chr7:12598209 | C | T | 6 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(3): Show |
6 | HG02970.hp2 HG03130.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-6305C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598209 | |||||||
chr7:12598235 | A | G | 1 | a0001c0001t0101g0122 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.517-6279A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598235 | |||||||
chr7:12598325 | G | A | 5 | a0001c0001t0054g0345 a0001c0001t0055g0348 a0001c0001t0071g0022 others(2): Show |
5 | HG00738.hp2 HG00741.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-6189G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598325 | |||||||
chr7:12598342 | C | G | 357 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.517-6172C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598342 | |||||||
chr7:12598443 | G | T | 10 | a0001c0001t0121g0201 a0002c0003t0006g0063 a0002c0003t0014g0069 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-6071G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598443 | |||||||
chr7:12598525 | A | G | 6 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0003t0006g0236 others(3): Show |
6 | HG00099.hp1 HG01433.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-5989A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598525 | |||||||
chr7:12598554 | GT | G | 7 | a0002c0003t0006g0234 a0002c0003t0017g0231 a0002c0003t0017g0233 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.517-5959delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598554 | |||||||
chr7:12598705 | C | A | 4 | a0002c0003t0006g0236 a0002c0003t0089g0235 a0002c0003t0134g0237 others(1): Show |
4 | HG02258.hp1 HG03225.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-5809C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598705 | |||||||
chr7:12598771 | T | C | 1 | a0007c0008t0003g0154 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.517-5743T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598771 | |||||||
chr7:12598789 | G | GTCCT | 5 | a0001c0001t0050g0349 a0002c0003t0015g0342 a0002c0003t0016g0339 others(2): Show |
5 | HG02109.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-5724_517-5721d others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12598789 | ||||||
chr7:12598799 | C | T | 10 | a0001c0001t0121g0201 a0002c0003t0006g0063 a0002c0003t0014g0069 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-5715C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598799 | |||||||
chr7:12598953 | A | G | 1 | a0002c0002t0157g0328 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.517-5561A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12598953 | |||||||
chr7:12599201 | A | G | 9 | a0002c0002t0001g0311 a0002c0002t0002g0320 a0002c0002t0002g0322 others(6): Show |
9 | HG00099.hp2 HG00323.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-5313A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12599201 | |||||||
chr7:12599370 | A | AGT | 5 | a0002c0003t0006g0337 a0002c0003t0015g0340 a0002c0003t0015g0342 others(2): Show |
5 | HG02109.hp1 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-5117_517-5116d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12599370 | ||||||
chr7:12599370 | A | AGTGT | 151 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(148): Show |
155 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.517-5119_517-5116d others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12599370 | ||||||
chr7:12599370 | A | AGTGTGT | 15 | a0001c0001t0002g0093 a0001c0001t0024g0131 a0001c0001t0030g0194 others(12): Show |
15 | HG00099.hp2 HG00408.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.517-5121_517-5116d others(8): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12599370 | ||||||
chr7:12599370 | AGT | A | 11 | a0001c0001t0027g0013 a0001c0001t0027g0042 a0001c0001t0179g0014 others(8): Show |
12 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.517-5117_517-5116d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12599370 | ||||||
chr7:12599370 | AGTGTGTG others(1): Show |
A | 46 | a0001c0001t0001g0159 a0001c0001t0003g0054 a0001c0001t0004g0108 others(43): Show |
46 | HG00544.hp2 HG01106.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.517-5123_517-5116d others(10): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12599370 | ||||||
chr7:12599371 | G | C | 1 | a0002c0002t0003g0305 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.517-5143G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12599371 | |||||||
chr7:12599488 | C | G | 45 | a0001c0001t0001g0159 a0001c0001t0003g0054 a0001c0001t0004g0108 others(42): Show |
45 | HG00544.hp2 HG01106.hp2 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.517-5026C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12599488 | |||||||
chr7:12599526 | A | G | 334 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(331): Show |
340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.517-4988A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12599526 | |||||||
chr7:12599596 | A | G | 4 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0002t0180g0245 others(1): Show |
4 | HG02280.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-4918A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12599596 | |||||||
chr7:12599614 | C | T | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.517-4900C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12599614 | |||||||
chr7:12599676 | A | G | 1 | a0002c0002t0174g0324 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.517-4838A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12599676 | |||||||
chr7:12599735 | G | A | 1 | a0001c0001t0172g0024 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.517-4779G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12599735 | |||||||
chr7:12599993 | T | C | 4 | a0004c0005t0006g0221 a0004c0005t0014g0202 a0004c0005t0042g0116 others(1): Show |
4 | HG00741.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-4521T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12599993 | |||||||
chr7:12600077 | G | A | 5 | a0002c0002t0004g0273 a0002c0002t0004g0290 a0002c0002t0005g0262 others(2): Show |
5 | HG00621.hp2 HG01346.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-4437G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12600077 | |||||||
chr7:12600197 | G | A | 1 | a0001c0001t0149g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.517-4317G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12600197 | |||||||
chr7:12600412 | G | A | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.517-4102G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12600412 | |||||||
chr7:12600447 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.517-4067A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12600447 | |||||||
chr7:12600480 | C | T | 343 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(340): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.517-4034C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12600480 | |||||||
chr7:12600529 | C | T | 8 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(5): Show |
8 | HG02886.hp1 HG02970.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.517-3985C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12600529 | |||||||
chr7:12600725 | C | A | 5 | a0002c0003t0006g0337 a0002c0003t0015g0340 a0002c0003t0015g0342 others(2): Show |
5 | HG02109.hp1 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-3789C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12600725 | |||||||
chr7:12600751 | T | G | 2 | a0010c0011t0031g0005 a0010c0011t0111g0005 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.517-3763T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12600751 | |||||||
chr7:12600865 | T | A | 334 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(331): Show |
340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.517-3649T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12600865 | |||||||
chr7:12600937 | A | G | 1 | a0004c0005t0042g0116 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.517-3577A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12600937 | |||||||
chr7:12601022 | C | T | 79 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(76): Show |
80 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.517-3492C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12601022 | |||||||
chr7:12601212 | G | A | 1 | a0002c0002t0158g0298 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.517-3302G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12601212 | |||||||
chr7:12601253 | G | A | 4 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0002t0180g0245 others(1): Show |
4 | HG02280.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-3261G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12601253 | |||||||
chr7:12601486 | A | G | 10 | a0001c0001t0121g0201 a0002c0003t0006g0063 a0002c0003t0014g0069 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-3028A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12601486 | |||||||
chr7:12601512 | G | A | 2 | a0008c0009t0159g0241 a0008c0009t0160g0243 |
2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517-3002G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12601512 | |||||||
chr7:12601577 | C | T | 79 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(76): Show |
80 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.517-2937C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12601577 | |||||||
chr7:12601719 | C | T | 2 | a0002c0002t0012g0278 a0002c0002t0015g0279 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.517-2795C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12601719 | |||||||
chr7:12601830 | T | C | 1 | a0002c0002t0012g0303 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.517-2684T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12601830 | |||||||
chr7:12601831 | T | A | 334 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(331): Show |
340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.517-2683T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12601831 | |||||||
chr7:12602052 | T | C | 3 | a0001c0001t0003g0181 a0001c0001t0003g0192 a0001c0001t0003g0217 |
3 | NA19010.hp1 NA19011.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.517-2462T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602052 | |||||||
chr7:12602057 | G | A | 2 | a0002c0003t0006g0063 a0008c0009t0110g0240 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.517-2457G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602057 | |||||||
chr7:12602064 | G | C | 2 | a0001c0001t0003g0083 a0001c0001t0003g0084 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.517-2450G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602064 | |||||||
chr7:12602102 | T | G | 1 | a0001c0001t0004g0128 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.517-2412T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602102 | |||||||
chr7:12602183 | A | G | 4 | a0002c0003t0006g0236 a0002c0003t0089g0235 a0002c0003t0134g0237 others(1): Show |
4 | HG02258.hp1 HG03225.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-2331A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602183 | |||||||
chr7:12602191 | A | G | 14 | a0001c0001t0121g0201 a0002c0003t0006g0063 a0002c0003t0006g0236 others(11): Show |
14 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.517-2323A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602191 | |||||||
chr7:12602210 | G | A | 1 | a0001c0001t0103g0089 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.517-2304G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602210 | |||||||
chr7:12602330 | T | G | 271 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(268): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.517-2184T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602330 | |||||||
chr7:12602334 | G | A | 1 | a0001c0001t0003g0182 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.517-2180G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602334 | |||||||
chr7:12602397 | A | G | 20 | a0001c0001t0054g0345 a0001c0001t0055g0348 a0001c0001t0071g0022 others(17): Show |
21 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.517-2117A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602397 | |||||||
chr7:12602437 | C | T | 1 | a0002c0003t0144g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.517-2077C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602437 | |||||||
chr7:12602451 | T | C | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.517-2063T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602451 | |||||||
chr7:12602547 | C | A | 5 | a0002c0003t0006g0337 a0002c0003t0015g0340 a0002c0003t0015g0342 others(2): Show |
5 | HG02109.hp1 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-1967C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12602547 | |||||||
chr7:12603036 | G | A | 5 | a0002c0003t0006g0337 a0002c0003t0015g0340 a0002c0003t0015g0342 others(2): Show |
5 | HG02109.hp1 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-1478G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12603036 | |||||||
chr7:12603176 | G | A | 2 | a0001c0001t0050g0349 a0010c0011t0135g0353 |
2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.517-1338G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12603176 | |||||||
chr7:12603305 | T | C | 357 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.517-1209T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12603305 | |||||||
chr7:12603386 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.517-1128G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12603386 | |||||||
chr7:12603516 | A | G | 1 | a0001c0001t0012g0106 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.517-998A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12603516 | |||||||
chr7:12603561 | C | G | 9 | a0002c0003t0006g0234 a0002c0003t0017g0231 a0002c0003t0017g0233 others(6): Show |
10 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.517-953C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12603561 | |||||||
chr7:12603565 | T | A | 1 | a0002c0002t0005g0262 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.517-949T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12603565 | |||||||
chr7:12603566 | C | G | 1 | a0002c0002t0005g0262 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.517-948C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12603566 | |||||||
chr7:12603653 | A | C | 17 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(14): Show |
17 | HG02109.hp1 HG02280.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.517-861A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12603653 | |||||||
chr7:12603767 | A | G | 7 | a0001c0001t0050g0349 a0002c0003t0006g0337 a0002c0003t0015g0340 others(4): Show |
7 | HG02109.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-747A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12603767 | |||||||
chr7:12603771 | T | C | 316 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(313): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.517-743T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12603771 | |||||||
chr7:12603909 | GT | G | 316 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(313): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.517-598delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 12603909 | ||||||
chr7:12604007 | T | C | 4 | a0006c0006t0007g0151 a0006c0006t0018g0176 a0006c0006t0139g0132 others(1): Show |
4 | NA18940.hp1 NA18945.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-507T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12604007 | |||||||
chr7:12604039 | T | C | 4 | a0001c0001t0014g0112 a0001c0001t0027g0013 a0001c0001t0027g0042 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-475T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12604039 | |||||||
chr7:12604099 | G | A | 357 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.517-415G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12604099 | |||||||
chr7:12604166 | A | G | 1 | a0002c0002t0001g0311 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.517-348A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12604166 | |||||||
chr7:12604171 | G | A | 1 | a0001c0001t0138g0080 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.517-343G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12604171 | |||||||
chr7:12604250 | T | C | 1 | a0001c0001t0023g0140 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.517-264T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12604250 | |||||||
chr7:12604408 | G | A | 180 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(177): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.517-106G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12604408 | |||||||
chr7:12604440 | A | G | 3 | a0002c0003t0089g0235 a0002c0003t0134g0237 a0002c0003t0161g0067 |
3 | HG02258.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.517-74A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 3/15 | chr7 | 12604440 | |||||||
chr7:12604685 | G | A | 1 | a0005c0007t0034g0350 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.666+22G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12604685 | |||||||
chr7:12604709 | G | T | 331 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(328): Show |
337 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.666+46G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12604709 | |||||||
chr7:12604723 | G | GGT | 331 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(328): Show |
337 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.666+75_666+76dupGT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12604723 | ||||||
chr7:12604750 | G | A | 4 | a0001c0001t0013g0020 a0001c0001t0153g0018 a0002c0002t0041g0325 others(1): Show |
4 | HG00642.hp1 HG01243.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+87G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12604750 | |||||||
chr7:12604874 | T | C | 13 | a0001c0001t0001g0029 a0001c0001t0009g0025 a0001c0001t0016g0023 others(10): Show |
13 | HG01175.hp2 HG02027.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.666+211T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12604874 | |||||||
chr7:12604875 | C | G | 4 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0002t0180g0245 others(1): Show |
4 | HG02280.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.666+212C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12604875 | |||||||
chr7:12604877 | T | C | 357 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.666+214T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12604877 | |||||||
chr7:12604925 | A | G | 2 | a0004c0005t0006g0221 a0004c0005t0042g0116 |
2 | HG00741.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.666+262A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12604925 | |||||||
chr7:12604931 | G | A | 1 | a0001c0001t0162g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.666+268G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12604931 | |||||||
chr7:12604991 | C | T | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.666+328C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12604991 | |||||||
chr7:12605005 | C | CT | 43 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(40): Show |
43 | HG00544.hp2 HG01106.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.666+345dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12605005 | ||||||
chr7:12605010 | A | T | 74 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(71): Show |
75 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.666+347A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605010 | |||||||
chr7:12605053 | T | G | 2 | a0002c0003t0006g0337 a0002c0003t0015g0340 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.666+390T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605053 | |||||||
chr7:12605137 | T | C | 1 | a0002c0003t0010g0287 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.666+474T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605137 | |||||||
chr7:12605177 | T | G | 12 | a0001c0001t0054g0345 a0001c0001t0055g0348 a0001c0001t0071g0022 others(9): Show |
12 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.666+514T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605177 | |||||||
chr7:12605208 | T | C | 1 | a0001c0001t0019g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.666+545T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605208 | |||||||
chr7:12605291 | C | T | 1 | a0013c0020t0038g0272 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.666+628C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605291 | |||||||
chr7:12605292 | G | A | 3 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0002t0175g0251 |
3 | HG00099.hp1 HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.666+629G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605292 | |||||||
chr7:12605295 | C | T | 6 | a0002c0002t0004g0273 a0002c0002t0004g0290 a0002c0002t0005g0262 others(3): Show |
6 | HG00621.hp2 HG01346.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+632C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605295 | |||||||
chr7:12605296 | G | T | 1 | a0002c0002t0015g0279 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.666+633G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605296 | |||||||
chr7:12605341 | G | T | 3 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0002t0175g0251 |
3 | HG00099.hp1 HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.666+678G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605341 | |||||||
chr7:12605436 | G | A | 1 | a0001c0001t0003g0119 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.666+773G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605436 | |||||||
chr7:12605467 | G | A | 1 | a0001c0001t0003g0193 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.666+804G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605467 | |||||||
chr7:12605521 | A | G | 1 | a0001c0001t0100g0222 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.666+858A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605521 | |||||||
chr7:12605574 | T | A | 10 | a0001c0001t0133g0198 a0001c0001t0141g0199 a0004c0005t0006g0221 others(7): Show |
10 | HG00738.hp1 HG00741.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.666+911T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605574 | |||||||
chr7:12605591 | A | C | 1 | a0002c0002t0005g0262 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.666+928A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605591 | |||||||
chr7:12605755 | A | G | 79 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(76): Show |
79 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.666+1092A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605755 | |||||||
chr7:12605996 | A | G | 357 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.666+1333A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12605996 | |||||||
chr7:12606362 | A | T | 185 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(182): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.666+1699A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12606362 | |||||||
chr7:12606679 | T | C | 2 | a0001c0001t0005g0164 a0001c0001t0005g0208 |
2 | NA18971.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.666+2016T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12606679 | |||||||
chr7:12606688 | G | A | 8 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0050g0349 others(5): Show |
8 | HG02970.hp2 HG02976.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.666+2025G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12606688 | |||||||
chr7:12606773 | A | T | 185 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(182): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.666+2110A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12606773 | |||||||
chr7:12606798 | T | G | 353 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(350): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.666+2135T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12606798 | |||||||
chr7:12606848 | T | C | 81 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(78): Show |
81 | HG00099.hp1 HG00544.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.666+2185T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12606848 | |||||||
chr7:12606947 | G | A | 1 | a0002c0002t0150g0318 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.666+2284G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12606947 | |||||||
chr7:12607014 | C | A | 2 | a0001c0001t0003g0182 a0001c0001t0070g0183 |
2 | HG01099.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.666+2351C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12607014 | |||||||
chr7:12607070 | G | A | 1 | a0004c0005t0106g0184 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.666+2407G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12607070 | |||||||
chr7:12607120 | G | A | 1 | a0001c0001t0003g0192 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.666+2457G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12607120 | |||||||
chr7:12607328 | C | A | 2 | a0002c0003t0015g0065 a0002c0003t0146g0062 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.666+2665C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12607328 | |||||||
chr7:12607505 | G | A | 4 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0003t0006g0236 others(1): Show |
4 | HG02280.hp2 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.666+2842G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12607505 | |||||||
chr7:12607753 | C | T | 1 | a0001c0001t0003g0181 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.666+3090C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12607753 | |||||||
chr7:12607760 | G | A | 2 | a0001c0001t0035g0104 a0001c0001t0151g0109 |
2 | NA18983.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.666+3097G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12607760 | |||||||
chr7:12607840 | G | A | 1 | a0008c0009t0006g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.666+3177G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12607840 | |||||||
chr7:12608308 | T | C | 189 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(186): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.666+3645T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12608308 | |||||||
chr7:12608310 | C | T | 2 | a0001c0001t0019g0166 a0001c0001t0154g0137 |
2 | HG00323.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.666+3647C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12608310 | |||||||
chr7:12608321 | G | GCA | 45 | a0001c0001t0001g0159 a0001c0001t0003g0054 a0001c0001t0004g0108 others(42): Show |
45 | HG00099.hp1 HG00544.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.666+3685_666+3686d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12608321 | ||||||
chr7:12608321 | G | GCACA | 10 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(7): Show |
10 | HG02109.hp1 HG03130.hp1 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.666+3683_666+3686d others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12608321 | ||||||
chr7:12608321 | G | GCACACA | 91 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(88): Show |
91 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.666+3681_666+3686d others(8): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12608321 | ||||||
chr7:12608321 | G | GCACACAC others(1): Show |
13 | a0001c0001t0002g0095 a0001c0001t0005g0139 a0001c0001t0005g0158 others(10): Show |
13 | HG01106.hp2 HG01109.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.666+3679_666+3686d others(10): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12608321 | ||||||
chr7:12608321 | G | GCACACAC others(5): Show |
2 | a0001c0001t0133g0198 a0001c0001t0141g0199 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.666+3675_666+3686d others(14): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12608321 | ||||||
chr7:12608321 | GCA | G | 175 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(172): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.666+3685_666+3686d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12608321 | ||||||
chr7:12608397 | C | T | 357 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.666+3734C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12608397 | |||||||
chr7:12608547 | G | A | 5 | a0001c0001t0003g0181 a0001c0001t0003g0192 a0001c0001t0003g0193 others(2): Show |
5 | NA19010.hp1 NA19011.hp1 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.666+3884G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12608547 | |||||||
chr7:12608627 | A | G | 13 | a0001c0001t0093g0043 a0002c0002t0012g0278 a0002c0002t0015g0279 others(10): Show |
13 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.666+3964A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12608627 | |||||||
chr7:12608653 | A | G | 3 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0002t0175g0251 |
3 | HG00099.hp1 HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.666+3990A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12608653 | |||||||
chr7:12608672 | T | C | 18 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0050g0349 others(15): Show |
18 | HG02109.hp1 HG02280.hp2 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.666+4009T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12608672 | |||||||
chr7:12608766 | C | T | 187 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(184): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.666+4103C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12608766 | |||||||
chr7:12608767 | G | A | 42 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(39): Show |
42 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.666+4104G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12608767 | |||||||
chr7:12608887 | G | A | 12 | a0001c0001t0176g0171 a0002c0002t0001g0308 a0002c0002t0001g0351 others(9): Show |
12 | HG00673.hp1 HG02071.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.666+4224G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12608887 | |||||||
chr7:12608933 | G | A | 4 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+4270G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12608933 | |||||||
chr7:12608989 | A | G | 182 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(179): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.666+4326A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12608989 | |||||||
chr7:12609183 | C | T | 3 | a0001c0001t0006g0016 a0001c0001t0014g0021 a0001c0001t0181g0017 |
3 | HG02630.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.666+4520C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609183 | |||||||
chr7:12609188 | G | T | 11 | a0001c0001t0003g0119 a0001c0001t0007g0051 a0001c0001t0011g0046 others(8): Show |
11 | HG00408.hp1 HG00438.hp1 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.666+4525G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609188 | |||||||
chr7:12609256 | G | A | 6 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+4593G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609256 | |||||||
chr7:12609345 | C | T | 41 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(38): Show |
41 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.666+4682C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609345 | |||||||
chr7:12609383 | G | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0101 others(33): Show |
37 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.666+4720G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609383 | |||||||
chr7:12609465 | C | T | 1 | a0002c0003t0060g0356 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.666+4802C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609465 | |||||||
chr7:12609527 | C | A | 1 | a0002c0002t0069g0269 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.666+4864C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609527 | |||||||
chr7:12609536 | C | A | 3 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0003t0047g0070 |
3 | HG02280.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.666+4873C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609536 | |||||||
chr7:12609577 | GA | G | 6 | a0001c0001t0010g0167 a0001c0001t0052g0343 a0001c0001t0053g0344 others(3): Show |
6 | HG01167.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.666+4921delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12609577 | ||||||
chr7:12609605 | A | G | 6 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+4942A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609605 | |||||||
chr7:12609697 | C | T | 3 | a0001c0001t0006g0016 a0001c0001t0014g0021 a0001c0001t0181g0017 |
3 | HG02630.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.666+5034C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609697 | |||||||
chr7:12609788 | A | G | 1 | a0002c0002t0002g0330 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.666+5125A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609788 | |||||||
chr7:12609831 | C | T | 1 | a0001c0001t0003g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.666+5168C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609831 | |||||||
chr7:12609875 | T | TA | 350 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(347): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.666+5221dupA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12609875 | ||||||
chr7:12609917 | A | G | 3 | a0002c0003t0089g0235 a0002c0003t0134g0237 a0002c0003t0161g0067 |
3 | HG02258.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.666+5254A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609917 | |||||||
chr7:12609943 | G | A | 4 | a0001c0001t0014g0112 a0001c0001t0027g0013 a0001c0001t0027g0042 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+5280G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609943 | |||||||
chr7:12609984 | G | A | 6 | a0002c0003t0006g0234 a0002c0003t0017g0231 a0002c0003t0017g0233 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.666+5321G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12609984 | |||||||
chr7:12610005 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0126 a0001c0001t0010g0150 others(2): Show |
5 | HG00621.hp1 HG02135.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+5342C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610005 | |||||||
chr7:12610337 | T | G | 5 | a0005c0007t0006g0335 a0005c0007t0034g0350 a0005c0007t0047g0338 others(2): Show |
6 | HG02145.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+5674T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610337 | |||||||
chr7:12610338 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.666+5675A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610338 | |||||||
chr7:12610372 | G | A | 109 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(106): Show |
109 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.666+5709G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610372 | |||||||
chr7:12610478 | T | C | 3 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0002t0175g0251 |
3 | HG00099.hp1 HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.666+5815T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610478 | |||||||
chr7:12610501 | T | C | 1 | a0001c0001t0100g0222 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.666+5838T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610501 | |||||||
chr7:12610573 | A | G | 1 | a0001c0001t0035g0033 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.666+5910A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610573 | |||||||
chr7:12610621 | C | T | 6 | a0001c0001t0093g0043 a0002c0003t0089g0235 a0002c0003t0134g0237 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.666+5958C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610621 | |||||||
chr7:12610681 | G | C | 2 | a0001c0001t0124g0185 a0002c0003t0036g0006 |
3 | HG01891.hp1 HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.666+6018G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610681 | |||||||
chr7:12610777 | G | C | 357 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.666+6114G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610777 | |||||||
chr7:12610805 | G | A | 357 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.666+6142G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610805 | |||||||
chr7:12610815 | T | C | 2 | a0001c0001t0124g0185 a0002c0003t0036g0006 |
3 | HG01891.hp1 HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.666+6152T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610815 | |||||||
chr7:12610954 | G | A | 3 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0002t0175g0251 |
3 | HG00099.hp1 HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.666+6291G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610954 | |||||||
chr7:12610986 | G | T | 1 | a0001c0001t0009g0056 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.666+6323G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12610986 | |||||||
chr7:12611226 | T | C | 180 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(177): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.666+6563T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12611226 | |||||||
chr7:12611234 | A | G | 3 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0003t0047g0070 |
3 | HG02280.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.666+6571A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12611234 | |||||||
chr7:12611253 | G | A | 3 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0003t0047g0070 |
3 | HG02280.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.666+6590G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12611253 | |||||||
chr7:12611453 | A | G | 185 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(182): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.666+6790A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12611453 | |||||||
chr7:12611573 | C | T | 7 | a0002c0002t0012g0278 a0002c0002t0015g0279 a0002c0003t0006g0337 others(4): Show |
7 | HG02109.hp1 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+6910C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12611573 | |||||||
chr7:12611588 | G | A | 3 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0002t0175g0251 |
3 | HG00099.hp1 HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.666+6925G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12611588 | |||||||
chr7:12611664 | G | A | 3 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0003t0047g0070 |
3 | HG02280.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.666+7001G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12611664 | |||||||
chr7:12611726 | A | G | 1 | a0001c0001t0043g0228 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.666+7063A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12611726 | |||||||
chr7:12611733 | G | A | 357 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.666+7070G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12611733 | |||||||
chr7:12611844 | C | G | 3 | a0001c0001t0005g0144 a0001c0001t0010g0142 a0002c0003t0022g0248 |
3 | HG03239.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.666+7181C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12611844 | |||||||
chr7:12611878 | T | C | 1 | a0002c0002t0001g0276 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.666+7215T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12611878 | |||||||
chr7:12611880 | T | G | 351 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(348): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.666+7217T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12611880 | |||||||
chr7:12611929 | TA | T | 231 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0029 others(228): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.666+7279delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12611929 | ||||||
chr7:12612008 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.666+7345T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612008 | |||||||
chr7:12612043 | CTGTACTT | C | 3 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0003t0047g0070 |
3 | HG02280.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.666+7385_666+7391d others(9): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12612043 | ||||||
chr7:12612058 | A | G | 88 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(85): Show |
93 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.666+7395A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612058 | |||||||
chr7:12612191 | G | A | 117 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(114): Show |
117 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.666+7528G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612191 | |||||||
chr7:12612205 | G | A | 2 | a0002c0002t0079g0280 a0017c0022t0034g0281 |
2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.666+7542G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612205 | |||||||
chr7:12612239 | C | G | 6 | a0006c0006t0007g0151 a0006c0006t0011g0152 a0006c0006t0018g0176 others(3): Show |
6 | NA18940.hp1 NA18945.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+7576C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612239 | |||||||
chr7:12612267 | G | A | 185 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(182): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.666+7604G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612267 | |||||||
chr7:12612369 | C | T | 2 | a0001c0001t0002g0087 a0001c0001t0138g0080 |
2 | NA18987.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.666+7706C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612369 | |||||||
chr7:12612519 | A | G | 3 | a0001c0001t0001g0146 a0002c0002t0010g0317 a0002c0002t0077g0314 |
3 | HG00735.hp2 HG02145.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.666+7856A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612519 | |||||||
chr7:12612576 | T | C | 43 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(40): Show |
43 | HG00544.hp2 HG01175.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.666+7913T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612576 | |||||||
chr7:12612580 | G | A | 1 | a0002c0002t0012g0303 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.666+7917G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612580 | |||||||
chr7:12612631 | T | C | 3 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0003t0047g0070 |
3 | HG02280.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.666+7968T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612631 | |||||||
chr7:12612712 | T | C | 10 | a0001c0001t0133g0198 a0001c0001t0141g0199 a0004c0005t0006g0221 others(7): Show |
10 | HG00738.hp1 HG00741.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.666+8049T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612712 | |||||||
chr7:12612753 | A | G | 3 | a0002c0002t0002g0239 a0002c0002t0078g0321 a0002c0002t0091g0292 |
3 | HG01978.hp2 HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.666+8090A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612753 | |||||||
chr7:12612770 | A | T | 1 | a0001c0001t0028g0047 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.666+8107A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612770 | |||||||
chr7:12612938 | G | A | 357 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.666+8275G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612938 | |||||||
chr7:12612943 | C | T | 1 | a0001c0001t0023g0140 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.666+8280C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12612943 | |||||||
chr7:12613020 | C | T | 1 | a0001c0001t0099g0103 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.666+8357C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12613020 | |||||||
chr7:12613122 | G | A | 2 | a0002c0002t0079g0280 a0017c0022t0034g0281 |
2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.666+8459G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12613122 | |||||||
chr7:12613173 | G | A | 6 | a0002c0003t0006g0234 a0002c0003t0017g0231 a0002c0003t0017g0233 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.666+8510G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12613173 | |||||||
chr7:12613420 | A | G | 68 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(65): Show |
68 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.666+8757A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12613420 | |||||||
chr7:12613434 | C | T | 3 | a0001c0001t0019g0230 a0002c0002t0013g0313 a0002c0002t0150g0318 |
3 | HG01175.hp2 HG03834.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.666+8771C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12613434 | |||||||
chr7:12613681 | G | A | 117 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(114): Show |
117 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.666+9018G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12613681 | |||||||
chr7:12613795 | A | C | 58 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(55): Show |
58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.667-9006A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12613795 | |||||||
chr7:12613900 | C | G | 1 | a0001c0001t0162g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.667-8901C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12613900 | |||||||
chr7:12613937 | A | G | 1 | a0001c0001t0033g0127 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.667-8864A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12613937 | |||||||
chr7:12614143 | T | C | 1 | a0009c0012t0080g0283 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.667-8658T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12614143 | |||||||
chr7:12614219 | T | A | 70 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(67): Show |
70 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.667-8582T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12614219 | |||||||
chr7:12614225 | G | C | 1 | a0004c0005t0006g0221 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.667-8576G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12614225 | |||||||
chr7:12614346 | A | T | 114 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(111): Show |
114 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.667-8455A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12614346 | |||||||
chr7:12614371 | C | T | 3 | a0002c0003t0089g0235 a0002c0003t0134g0237 a0002c0003t0161g0067 |
3 | HG02258.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.667-8430C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12614371 | |||||||
chr7:12614398 | C | T | 1 | a0002c0002t0001g0276 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.667-8403C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12614398 | |||||||
chr7:12614406 | G | A | 84 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(81): Show |
84 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.667-8395G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12614406 | |||||||
chr7:12614413 | T | C | 1 | a0002c0002t0065g0297 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.667-8388T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12614413 | |||||||
chr7:12614549 | G | A | 30 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(27): Show |
30 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.667-8252G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12614549 | |||||||
chr7:12614654 | A | G | 45 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(42): Show |
45 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.667-8147A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12614654 | |||||||
chr7:12614945 | A | G | 181 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(178): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.667-7856A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12614945 | |||||||
chr7:12615030 | A | G | 45 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(42): Show |
45 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.667-7771A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615030 | |||||||
chr7:12615035 | A | G | 1 | a0001c0001t0138g0080 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.667-7766A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615035 | |||||||
chr7:12615071 | C | T | 113 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(110): Show |
113 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.667-7730C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615071 | |||||||
chr7:12615149 | G | T | 3 | a0002c0003t0089g0235 a0002c0003t0134g0237 a0002c0003t0161g0067 |
3 | HG02258.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.667-7652G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615149 | |||||||
chr7:12615155 | T | C | 1 | a0004c0005t0104g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.667-7646T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615155 | |||||||
chr7:12615240 | T | A | 3 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0003t0047g0070 |
3 | HG02280.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.667-7561T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615240 | |||||||
chr7:12615360 | G | A | 45 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(42): Show |
45 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.667-7441G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615360 | |||||||
chr7:12615418 | T | G | 357 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.667-7383T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615418 | |||||||
chr7:12615456 | C | T | 1 | a0001c0001t0013g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.667-7345C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615456 | |||||||
chr7:12615480 | G | A | 41 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(38): Show |
41 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.667-7321G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615480 | |||||||
chr7:12615525 | G | C | 2 | a0002c0003t0015g0065 a0002c0003t0146g0062 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.667-7276G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615525 | |||||||
chr7:12615567 | C | G | 6 | a0002c0003t0006g0234 a0002c0003t0017g0231 a0002c0003t0017g0233 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.667-7234C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615567 | |||||||
chr7:12615629 | T | C | 5 | a0002c0003t0006g0337 a0002c0003t0015g0340 a0002c0003t0015g0342 others(2): Show |
5 | HG02109.hp1 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.667-7172T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615629 | |||||||
chr7:12615673 | G | A | 3 | a0002c0003t0089g0235 a0002c0003t0134g0237 a0002c0003t0161g0067 |
3 | HG02258.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.667-7128G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615673 | |||||||
chr7:12615703 | T | G | 3 | a0001c0001t0185g0200 a0008c0009t0159g0241 a0008c0009t0160g0243 |
3 | HG02572.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.667-7098T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615703 | |||||||
chr7:12615736 | G | A | 3 | a0001c0001t0112g0178 a0002c0010t0068g0265 a0002c0010t0128g0266 |
3 | HG01106.hp2 HG01952.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.667-7065G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615736 | |||||||
chr7:12615863 | C | G | 14 | a0001c0001t0121g0201 a0001c0001t0185g0200 a0002c0002t0180g0245 others(11): Show |
14 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.667-6938C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12615863 | |||||||
chr7:12616052 | G | T | 1 | a0001c0001t0123g0057 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.667-6749G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616052 | |||||||
chr7:12616086 | A | T | 2 | a0002c0002t0079g0280 a0017c0022t0034g0281 |
2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.667-6715A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616086 | |||||||
chr7:12616198 | G | C | 1 | a0001c0001t0166g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.667-6603G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616198 | |||||||
chr7:12616287 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.667-6514T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616287 | |||||||
chr7:12616400 | A | G | 5 | a0001c0001t0003g0182 a0001c0001t0070g0183 a0002c0002t0002g0329 others(2): Show |
5 | HG01099.hp2 HG01884.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.667-6401A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616400 | |||||||
chr7:12616528 | T | C | 1 | a0001c0001t0003g0002 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.667-6273T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616528 | |||||||
chr7:12616535 | A | T | 82 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(79): Show |
82 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.667-6266A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616535 | |||||||
chr7:12616636 | C | G | 1 | a0002c0003t0006g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.667-6165C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616636 | |||||||
chr7:12616722 | A | G | 1 | a0008c0009t0006g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.667-6079A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616722 | |||||||
chr7:12616737 | T | C | 1 | a0001c0001t0016g0023 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.667-6064T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616737 | |||||||
chr7:12616779 | G | A | 1 | a0002c0002t0002g0330 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.667-6022G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616779 | |||||||
chr7:12616790 | A | G | 45 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(42): Show |
45 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.667-6011A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616790 | |||||||
chr7:12616856 | T | C | 1 | a0002c0002t0065g0297 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.667-5945T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616856 | |||||||
chr7:12616870 | A | C | 2 | a0001c0001t0023g0162 a0001c0001t0152g0161 |
2 | HG02155.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.667-5931A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616870 | |||||||
chr7:12616883 | A | G | 1 | a0002c0002t0084g0259 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.667-5918A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12616883 | |||||||
chr7:12617097 | G | A | 81 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(78): Show |
81 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.667-5704G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12617097 | |||||||
chr7:12617139 | G | C | 1 | a0001c0001t0124g0185 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.667-5662G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12617139 | |||||||
chr7:12617158 | G | C | 1 | a0001c0001t0016g0023 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.667-5643G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12617158 | |||||||
chr7:12617452 | G | A | 1 | a0001c0001t0073g0036 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.667-5349G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12617452 | |||||||
chr7:12617513 | G | C | 1 | a0001c0001t0010g0142 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.667-5288G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12617513 | |||||||
chr7:12617516 | T | G | 1 | a0001c0001t0179g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.667-5285T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12617516 | |||||||
chr7:12617577 | C | A | 3 | a0002c0003t0089g0235 a0002c0003t0134g0237 a0002c0003t0161g0067 |
3 | HG02258.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.667-5224C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12617577 | |||||||
chr7:12617696 | C | G | 3 | a0002c0003t0089g0235 a0002c0003t0134g0237 a0002c0003t0161g0067 |
3 | HG02258.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.667-5105C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12617696 | |||||||
chr7:12618121 | A | C | 187 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(184): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.667-4680A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12618121 | |||||||
chr7:12618262 | G | A | 3 | a0002c0003t0089g0235 a0002c0003t0134g0237 a0002c0003t0161g0067 |
3 | HG02258.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.667-4539G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12618262 | |||||||
chr7:12618662 | T | C | 46 | a0001c0001t0001g0124 a0001c0001t0001g0159 a0001c0001t0002g0095 others(43): Show |
46 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.667-4139T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12618662 | |||||||
chr7:12618745 | C | A | 1 | a0005c0007t0034g0350 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.667-4056C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12618745 | |||||||
chr7:12618820 | G | T | 1 | a0002c0003t0015g0340 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.667-3981G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12618820 | |||||||
chr7:12618923 | C | G | 10 | a0001c0001t0004g0108 a0001c0001t0018g0110 a0001c0001t0018g0187 others(7): Show |
10 | HG02004.hp1 HG02165.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.667-3878C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12618923 | |||||||
chr7:12618992 | A | G | 2 | a0001c0001t0022g0174 a0001c0001t0022g0175 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.667-3809A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12618992 | |||||||
chr7:12618993 | C | G | 6 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(3): Show |
6 | HG02970.hp2 HG03130.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.667-3808C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12618993 | |||||||
chr7:12619106 | A | G | 4 | a0001c0001t0066g0045 a0002c0002t0031g0285 a0002c0003t0059g0362 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-3695A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619106 | |||||||
chr7:12619127 | G | A | 2 | a0001c0001t0133g0198 a0001c0001t0141g0199 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.667-3674G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619127 | |||||||
chr7:12619313 | A | G | 1 | a0017c0022t0034g0281 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.667-3488A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619313 | |||||||
chr7:12619318 | G | A | 5 | a0002c0003t0006g0337 a0002c0003t0015g0340 a0002c0003t0015g0342 others(2): Show |
5 | HG02109.hp1 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.667-3483G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619318 | |||||||
chr7:12619355 | T | C | 82 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(79): Show |
82 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.667-3446T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619355 | |||||||
chr7:12619409 | C | A | 1 | a0001c0001t0020g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.667-3392C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619409 | |||||||
chr7:12619462 | C | G | 6 | a0001c0001t0093g0043 a0002c0003t0089g0235 a0002c0003t0134g0237 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.667-3339C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619462 | |||||||
chr7:12619543 | T | C | 5 | a0005c0007t0006g0335 a0005c0007t0034g0350 a0005c0007t0047g0338 others(2): Show |
6 | HG02145.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-3258T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619543 | |||||||
chr7:12619628 | T | C | 98 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(95): Show |
98 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.667-3173T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619628 | |||||||
chr7:12619690 | A | G | 2 | a0001c0001t0019g0166 a0001c0001t0154g0137 |
2 | HG00323.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.667-3111A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619690 | |||||||
chr7:12619769 | T | A | 357 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.667-3032T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619769 | |||||||
chr7:12619776 | C | A | 8 | a0001c0001t0001g0029 a0001c0001t0009g0025 a0001c0001t0012g0106 others(5): Show |
8 | HG02027.hp2 NA18949.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.667-3025C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619776 | |||||||
chr7:12619776 | C | G | 1 | a0002c0002t0150g0318 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.667-3025C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619776 | |||||||
chr7:12619801 | C | A | 1 | a0011c0013t0014g0238 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.667-3000C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619801 | |||||||
chr7:12619840 | C | T | 189 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(186): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.667-2961C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619840 | |||||||
chr7:12619925 | A | G | 1 | a0001c0001t0183g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.667-2876A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619925 | |||||||
chr7:12619985 | A | T | 6 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-2816A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12619985 | |||||||
chr7:12620056 | A | G | 4 | a0001c0001t0173g0081 a0002c0002t0002g0247 a0002c0002t0020g0244 others(1): Show |
4 | HG00438.hp1 HG02280.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-2745A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12620056 | |||||||
chr7:12620073 | C | T | 1 | a0001c0001t0067g0205 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.667-2728C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12620073 | |||||||
chr7:12620286 | CT | C | 9 | a0001c0001t0001g0029 a0001c0001t0009g0025 a0001c0001t0012g0106 others(6): Show |
9 | HG02027.hp2 NA18949.hp2 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-2512delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12620286 | ||||||
chr7:12620388 | A | G | 3 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0002t0175g0251 |
3 | HG00099.hp1 HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.667-2413A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12620388 | |||||||
chr7:12620433 | A | G | 1 | a0001c0001t0024g0098 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.667-2368A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12620433 | |||||||
chr7:12620581 | C | T | 1 | a0002c0002t0001g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.667-2220C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12620581 | |||||||
chr7:12620901 | C | T | 275 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(272): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.667-1900C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12620901 | |||||||
chr7:12620939 | G | C | 2 | a0002c0002t0012g0278 a0002c0002t0015g0279 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-1862G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12620939 | |||||||
chr7:12620968 | A | G | 1 | a0001c0001t0095g0039 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.667-1833A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12620968 | |||||||
chr7:12620984 | A | G | 6 | a0002c0003t0006g0234 a0002c0003t0017g0231 a0002c0003t0017g0233 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.667-1817A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12620984 | |||||||
chr7:12621130 | G | A | 1 | a0002c0002t0169g0293 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.667-1671G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621130 | |||||||
chr7:12621269 | T | C | 1 | a0002c0003t0006g0337 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.667-1532T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621269 | |||||||
chr7:12621458 | A | T | 1 | a0002c0002t0005g0319 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.667-1343A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621458 | |||||||
chr7:12621473 | A | G | 6 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-1328A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621473 | |||||||
chr7:12621484 | T | G | 4 | a0004c0005t0019g0177 a0004c0005t0049g0346 a0004c0005t0104g0138 others(1): Show |
4 | HG00738.hp1 HG01978.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-1317T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621484 | |||||||
chr7:12621548 | A | G | 1 | a0002c0002t0113g0277 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.667-1253A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621548 | |||||||
chr7:12621637 | G | GT | 11 | a0001c0001t0014g0112 a0001c0001t0163g0035 a0002c0002t0002g0247 others(8): Show |
11 | HG00741.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.667-1144dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12621637 | ||||||
chr7:12621637 | G | GTT | 8 | a0001c0001t0066g0045 a0002c0002t0012g0334 a0002c0002t0031g0285 others(5): Show |
8 | HG00738.hp1 HG01243.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-1145_667-1144d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12621637 | ||||||
chr7:12621637 | G | GTTT | 32 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0004g0108 others(29): Show |
32 | HG01175.hp1 HG01256.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.667-1146_667-1144d others(5): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12621637 | ||||||
chr7:12621637 | G | GTTTT | 10 | a0001c0001t0003g0054 a0001c0001t0005g0139 a0001c0001t0029g0076 others(7): Show |
10 | HG00544.hp2 HG01106.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.667-1147_667-1144d others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12621637 | ||||||
chr7:12621637 | GT | G | 92 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(89): Show |
92 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.667-1144delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12621637 | ||||||
chr7:12621637 | GTT | G | 180 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(177): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.667-1145_667-1144d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12621637 | ||||||
chr7:12621643 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.667-1158T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621643 | |||||||
chr7:12621646 | T | A | 1 | a0001c0001t0118g0049 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.667-1155T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621646 | |||||||
chr7:12621646 | T | G | 1 | a0002c0002t0005g0262 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.667-1155T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621646 | |||||||
chr7:12621647 | T | G | 1 | a0001c0001t0118g0049 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.667-1154T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621647 | |||||||
chr7:12621687 | A | G | 8 | a0004c0005t0006g0221 a0004c0005t0014g0202 a0004c0005t0019g0177 others(5): Show |
8 | HG00738.hp1 HG00741.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.667-1114A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621687 | |||||||
chr7:12621866 | G | A | 1 | a0001c0001t0009g0056 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.667-935G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621866 | |||||||
chr7:12621884 | C | T | 1 | a0002c0002t0012g0303 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.667-917C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621884 | |||||||
chr7:12621941 | G | A | 6 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-860G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12621941 | |||||||
chr7:12622051 | C | G | 6 | a0002c0002t0004g0273 a0002c0002t0004g0290 a0002c0002t0005g0262 others(3): Show |
6 | HG00621.hp2 HG01346.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-750C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12622051 | |||||||
chr7:12622124 | T | C | 1 | a0002c0002t0177g0263 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.667-677T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12622124 | |||||||
chr7:12622141 | C | A | 7 | a0001c0001t0003g0054 a0006c0006t0007g0151 a0006c0006t0011g0152 others(4): Show |
7 | HG03669.hp1 NA18940.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.667-660C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12622141 | |||||||
chr7:12622169 | CT | C | 6 | a0001c0001t0093g0043 a0002c0003t0089g0235 a0002c0003t0134g0237 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.667-626delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 12622169 | ||||||
chr7:12622304 | G | A | 1 | a0007c0008t0003g0154 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.667-497G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12622304 | |||||||
chr7:12622587 | A | G | 30 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(27): Show |
30 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.667-214A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12622587 | |||||||
chr7:12622597 | C | T | 1 | a0002c0003t0057g0360 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.667-204C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12622597 | |||||||
chr7:12622682 | G | A | 3 | a0001c0001t0093g0043 a0010c0011t0031g0005 a0010c0011t0111g0005 |
3 | HG02055.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.667-119G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 4/15 | chr7 | 12622682 | |||||||
chr7:12622925 | A | C | 6 | a0001c0001t0093g0043 a0002c0003t0089g0235 a0002c0003t0134g0237 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+32A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12622925 | |||||||
chr7:12622978 | G | A | 9 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0003g0037 others(6): Show |
9 | HG02015.hp1 HG02165.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.759+85G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12622978 | |||||||
chr7:12623240 | C | G | 1 | a0001c0001t0003g0182 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.759+347C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12623240 | |||||||
chr7:12623612 | G | C | 3 | a0001c0001t0093g0043 a0010c0011t0031g0005 a0010c0011t0111g0005 |
3 | HG02055.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.759+719G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12623612 | |||||||
chr7:12623638 | C | G | 3 | a0009c0012t0080g0283 a0009c0012t0082g0284 a0009c0012t0085g0282 |
3 | HG02257.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.759+745C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12623638 | |||||||
chr7:12623666 | C | T | 14 | a0001c0001t0121g0201 a0001c0001t0185g0200 a0002c0002t0180g0245 others(11): Show |
14 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.759+773C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12623666 | |||||||
chr7:12623894 | A | G | 6 | a0001c0001t0093g0043 a0002c0003t0089g0235 a0002c0003t0134g0237 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+1001A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12623894 | |||||||
chr7:12624275 | C | G | 3 | a0002c0002t0001g0258 a0002c0002t0012g0334 a0002c0002t0084g0259 |
3 | NA18944.hp1 NA18952.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.760-735C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12624275 | |||||||
chr7:12624327 | A | G | 1 | a0001c0001t0029g0076 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.760-683A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12624327 | |||||||
chr7:12624493 | A | G | 246 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(243): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.760-517A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12624493 | |||||||
chr7:12624626 | A | G | 43 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(40): Show |
43 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.760-384A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12624626 | |||||||
chr7:12624806 | T | A | 1 | a0001c0001t0108g0204 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.760-204T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12624806 | |||||||
chr7:12624817 | C | A | 1 | a0001c0001t0107g0097 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.760-193C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12624817 | |||||||
chr7:12624896 | A | G | 1 | a0001c0001t0108g0204 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.760-114A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 5/15 | chr7 | 12624896 | |||||||
chr7:12625187 | T | C | 1 | a0001c0001t0014g0112 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.892+45T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | chr7 | 12625187 | |||||||
chr7:12625271 | T | C | 41 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(38): Show |
41 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.892+129T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | chr7 | 12625271 | |||||||
chr7:12625272 | C | T | 1 | a0004c0005t0049g0346 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.892+130C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | chr7 | 12625272 | |||||||
chr7:12625378 | G | A | 1 | a0002c0002t0001g0276 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.892+236G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | chr7 | 12625378 | |||||||
chr7:12625431 | C | CT | 193 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0029 others(190): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.892+309dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr7 | 12625431 | ||||||
chr7:12625431 | C | CTT | 150 | a0001c0001t0001g0027 a0001c0001t0001g0079 a0001c0001t0001g0088 others(147): Show |
150 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.892+308_892+309dup others(2): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr7 | 12625431 | ||||||
chr7:12625431 | C | CTTT | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0010g0142 others(7): Show |
10 | HG00621.hp1 HG01167.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.892+307_892+309dup others(3): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr7 | 12625431 | ||||||
chr7:12625451 | T | TTTC | 8 | a0001c0001t0083g0118 a0004c0005t0006g0221 a0004c0005t0014g0202 others(5): Show |
8 | HG00738.hp1 HG00741.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.892+309_892+310ins others(3): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | chr7 | 12625451 | |||||||
chr7:12625495 | A | AT | 6 | a0001c0001t0093g0043 a0002c0003t0089g0235 a0002c0003t0134g0237 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.893-260dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr7 | 12625495 | ||||||
chr7:12625505 | A | AT | 6 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.893-251dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr7 | 12625505 | ||||||
chr7:12625533 | G | C | 22 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(19): Show |
22 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.893-229G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | chr7 | 12625533 | |||||||
chr7:12625584 | T | C | 239 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(236): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.893-178T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | chr7 | 12625584 | |||||||
chr7:12625609 | G | A | 1 | a0001c0001t0066g0045 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.893-153G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 6/15 | chr7 | 12625609 | |||||||
chr7:12625874 | A | G | 1 | a0001c0001t0032g0082 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.981+24A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 7/15 | chr7 | 12625874 | |||||||
chr7:12625892 | T | C | 47 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(44): Show |
47 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.981+42T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 7/15 | chr7 | 12625892 | |||||||
chr7:12625913 | C | T | 3 | a0002c0002t0002g0247 a0002c0002t0020g0244 a0002c0003t0047g0070 |
3 | HG02280.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.981+63C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 7/15 | chr7 | 12625913 | |||||||
chr7:12625946 | G | A | 1 | a0002c0003t0047g0070 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.981+96G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 7/15 | chr7 | 12625946 | |||||||
chr7:12626114 | G | A | 191 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(188): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.981+264G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 7/15 | chr7 | 12626114 | |||||||
chr7:12626165 | A | G | 1 | a0002c0002t0018g0296 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.981+315A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 7/15 | chr7 | 12626165 | |||||||
chr7:12626242 | G | A | 3 | a0001c0001t0124g0185 a0001c0001t0132g0186 a0002c0003t0036g0006 |
4 | HG01081.hp2 HG01891.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.982-342G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 7/15 | chr7 | 12626242 | |||||||
chr7:12626337 | C | T | 2 | a0001c0001t0099g0103 a0001c0001t0173g0081 |
2 | HG00438.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.982-247C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 7/15 | chr7 | 12626337 | |||||||
chr7:12626341 | T | G | 1 | a0002c0003t0063g0357 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.982-243T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 7/15 | chr7 | 12626341 | |||||||
chr7:12626915 | C | T | 47 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(44): Show |
47 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.1197+116C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12626915 | |||||||
chr7:12626948 | G | A | 2 | a0001c0001t0136g0117 a0002c0002t0113g0277 |
2 | HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1197+149G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12626948 | |||||||
chr7:12627091 | T | C | 1 | a0002c0003t0006g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1197+292T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627091 | |||||||
chr7:12627091 | T | TAC | 195 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1197+314_1197+315d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 12627091 | ||||||
chr7:12627091 | T | TACAC | 62 | a0001c0001t0001g0055 a0001c0001t0003g0119 a0001c0001t0007g0051 others(59): Show |
62 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1197+312_1197+315d others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 12627091 | ||||||
chr7:12627138 | A | T | 2 | a0002c0002t0129g0007 a0002c0002t0130g0007 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1197+339A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627138 | |||||||
chr7:12627250 | G | C | 186 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(183): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1197+451G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627250 | |||||||
chr7:12627282 | A | G | 233 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0048 others(230): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1197+483A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627282 | |||||||
chr7:12627430 | A | C | 1 | a0001c0001t0067g0205 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1197+631A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627430 | |||||||
chr7:12627454 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1197+655C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627454 | |||||||
chr7:12627496 | G | C | 3 | a0002c0003t0089g0235 a0002c0003t0134g0237 a0002c0003t0161g0067 |
3 | HG02258.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1197+697G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627496 | |||||||
chr7:12627578 | A | G | 1 | a0002c0003t0015g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1197+779A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627578 | |||||||
chr7:12627583 | G | C | 69 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0079 others(66): Show |
69 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1197+784G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627583 | |||||||
chr7:12627647 | T | C | 2 | a0001c0001t0037g0012 a0001c0001t0166g0011 |
2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1197+848T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627647 | |||||||
chr7:12627714 | G | T | 7 | a0002c0002t0079g0280 a0005c0007t0006g0335 a0005c0007t0034g0350 others(4): Show |
8 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1197+915G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627714 | |||||||
chr7:12627715 | G | A | 50 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(47): Show |
50 | HG00099.hp1 HG00544.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.1197+916G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627715 | |||||||
chr7:12627863 | C | A | 1 | a0002c0003t0089g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1197+1064C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627863 | |||||||
chr7:12627949 | C | T | 3 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0002t0175g0251 |
3 | HG00099.hp1 HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1197+1150C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627949 | |||||||
chr7:12627993 | T | G | 1 | a0002c0003t0089g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1198-1108T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12627993 | |||||||
chr7:12628026 | TGC | T | 4 | a0001c0001t0090g0015 a0001c0001t0096g0050 a0001c0001t0102g0188 others(1): Show |
4 | HG01167.hp2 HG01891.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-1069_1198-106 others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 12628026 | ||||||
chr7:12628029 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1198-1072G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628029 | |||||||
chr7:12628030 | C | T | 1 | a0002c0003t0089g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1198-1071C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628030 | |||||||
chr7:12628030 | CGCGTGTG others(3): Show |
C | 8 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(5): Show |
8 | HG02886.hp1 HG02970.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1198-1069_1198-106 others(14): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 12628030 | ||||||
chr7:12628030 | CGCGTGTG others(5): Show |
C | 5 | a0002c0003t0006g0337 a0002c0003t0015g0340 a0002c0003t0015g0342 others(2): Show |
5 | HG02109.hp1 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-1069_1198-105 others(16): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 12628030 | ||||||
chr7:12628032 | C | CGT | 5 | a0001c0001t0009g0056 a0002c0003t0144g0072 a0009c0012t0080g0283 others(2): Show |
5 | HG02109.hp2 HG02257.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-1036_1198-103 others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 12628032 | ||||||
chr7:12628032 | C | T | 1 | a0002c0003t0089g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1198-1069C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628032 | |||||||
chr7:12628032 | CGT | C | 161 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(158): Show |
162 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1198-1036_1198-103 others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 12628032 | ||||||
chr7:12628032 | CGTGT | C | 137 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(134): Show |
142 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1198-1038_1198-103 others(8): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 12628032 | ||||||
chr7:12628032 | CGTGTGT | C | 12 | a0001c0001t0005g0144 a0001c0001t0010g0167 a0001c0001t0185g0200 others(9): Show |
12 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1198-1040_1198-103 others(10): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 12628032 | ||||||
chr7:12628032 | CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0107g0097 a0001c0001t0179g0014 a0002c0002t0001g0252 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-1042_1198-103 others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 12628032 | ||||||
chr7:12628034 | T | C | 1 | a0001c0001t0093g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1198-1067T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628034 | |||||||
chr7:12628036 | T | C | 5 | a0001c0001t0145g0041 a0002c0002t0065g0297 a0003c0004t0004g0133 others(2): Show |
5 | HG02004.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-1065T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628036 | |||||||
chr7:12628038 | T | C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(80): Show |
87 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1198-1063T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628038 | |||||||
chr7:12628040 | T | C | 3 | a0001c0001t0075g0179 a0001c0001t0185g0200 a0008c0009t0160g0243 |
3 | HG02572.hp1 HG03486.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.1198-1061T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628040 | |||||||
chr7:12628042 | T | C | 5 | a0001c0001t0107g0097 a0001c0001t0179g0014 a0002c0002t0001g0252 others(2): Show |
5 | HG00099.hp1 HG01433.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-1059T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628042 | |||||||
chr7:12628044 | T | C | 3 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0002t0175g0251 |
3 | HG00099.hp1 HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1198-1057T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628044 | |||||||
chr7:12628046 | T | C | 3 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0002t0175g0251 |
3 | HG00099.hp1 HG01433.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1198-1055T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628046 | |||||||
chr7:12628109 | G | A | 1 | a0002c0003t0089g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1198-992G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628109 | |||||||
chr7:12628162 | G | C | 203 | a0001c0001t0001g0029 a0001c0001t0001g0055 a0001c0001t0001g0146 others(200): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1198-939G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628162 | |||||||
chr7:12628241 | A | T | 1 | a0001c0001t0170g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1198-860A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628241 | |||||||
chr7:12628252 | G | C | 1 | a0002c0002t0001g0308 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1198-849G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628252 | |||||||
chr7:12628276 | A | G | 1 | a0001c0001t0083g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1198-825A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628276 | |||||||
chr7:12628410 | G | T | 1 | a0001c0001t0045g0053 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1198-691G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628410 | |||||||
chr7:12628532 | C | T | 3 | a0001c0001t0003g0083 a0001c0001t0003g0084 a0001c0001t0032g0082 |
3 | HG00140.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1198-569C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628532 | |||||||
chr7:12628584 | G | A | 9 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0003g0037 others(6): Show |
9 | HG02015.hp1 HG02165.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.1198-517G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628584 | |||||||
chr7:12628719 | T | A | 45 | a0001c0001t0001g0146 a0001c0001t0003g0182 a0001c0001t0013g0020 others(42): Show |
46 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1198-382T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12628719 | |||||||
chr7:12629098 | C | T | 1 | a0001c0001t0094g0102 | 1 | HG00423.hp1 | splice_region_variant&intron_variant | LOW | c.1198-3C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 8/15 | chr7 | 12629098 | |||||||
chr7:12629391 | T | C | 274 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1319+169T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12629391 | |||||||
chr7:12629398 | C | CCA | 120 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(117): Show |
125 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1319+179_1319+180d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12629398 | ||||||
chr7:12629544 | G | C | 2 | a0001c0001t0074g0052 a0001c0001t0075g0179 |
2 | NA18939.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.1319+322G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12629544 | |||||||
chr7:12629583 | A | G | 10 | a0004c0005t0006g0221 a0004c0005t0014g0202 a0004c0005t0019g0177 others(7): Show |
10 | HG00738.hp1 HG00741.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1319+361A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12629583 | |||||||
chr7:12629626 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(69): Show |
76 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1319+404G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12629626 | |||||||
chr7:12630313 | C | A | 1 | a0002c0010t0001g0261 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1319+1091C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12630313 | |||||||
chr7:12630415 | G | C | 1 | a0001c0001t0066g0045 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1319+1193G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12630415 | |||||||
chr7:12630454 | A | G | 46 | a0001c0001t0001g0146 a0001c0001t0003g0182 a0001c0001t0013g0020 others(43): Show |
47 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1319+1232A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12630454 | |||||||
chr7:12630621 | G | A | 10 | a0004c0005t0006g0221 a0004c0005t0014g0202 a0004c0005t0019g0177 others(7): Show |
10 | HG00738.hp1 HG00741.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1319+1399G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12630621 | |||||||
chr7:12630633 | G | A | 3 | a0002c0002t0002g0329 a0002c0002t0002g0330 a0002c0002t0002g0332 |
3 | HG03491.hp2 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1319+1411G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12630633 | |||||||
chr7:12630676 | A | C | 34 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(31): Show |
35 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.1319+1454A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12630676 | |||||||
chr7:12630777 | G | T | 3 | a0001c0001t0001g0121 a0001c0001t0002g0169 a0001c0001t0108g0204 |
3 | HG01099.hp1 HG01123.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1319+1555G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12630777 | |||||||
chr7:12630995 | T | C | 1 | a0002c0003t0006g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1319+1773T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12630995 | |||||||
chr7:12631078 | T | G | 74 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(71): Show |
78 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1319+1856T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12631078 | |||||||
chr7:12631177 | T | A | 2 | a0002c0014t0006g0060 a0002c0014t0184g0059 |
2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1319+1955T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12631177 | |||||||
chr7:12631179 | A | C | 1 | a0001c0001t0103g0089 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1319+1957A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12631179 | |||||||
chr7:12631307 | G | A | 1 | a0001c0001t0010g0167 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1319+2085G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12631307 | |||||||
chr7:12631344 | C | G | 1 | a0002c0003t0060g0356 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1319+2122C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12631344 | |||||||
chr7:12631369 | C | G | 2 | a0001c0001t0011g0034 a0019c0015t0013g0038 |
2 | NA18964.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1319+2147C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12631369 | |||||||
chr7:12631442 | A | G | 2 | a0002c0003t0089g0235 a0002c0003t0161g0067 |
2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1319+2220A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12631442 | |||||||
chr7:12631457 | T | A | 6 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1319+2235T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12631457 | |||||||
chr7:12631475 | A | C | 1 | a0001c0001t0017g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1319+2253A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12631475 | |||||||
chr7:12631908 | A | G | 46 | a0001c0001t0001g0146 a0001c0001t0003g0182 a0001c0001t0013g0020 others(43): Show |
47 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1319+2686A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12631908 | |||||||
chr7:12631977 | C | T | 98 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(95): Show |
98 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1319+2755C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12631977 | |||||||
chr7:12632083 | C | CATTTT | 83 | a0001c0001t0001g0055 a0001c0001t0001g0091 a0001c0001t0001g0146 others(80): Show |
83 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1319+2923_1319+292 others(9): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12632083 | ||||||
chr7:12632083 | C | CATTTTAT others(3): Show |
22 | a0001c0001t0001g0048 a0001c0001t0003g0054 a0001c0001t0003g0192 others(19): Show |
22 | HG00544.hp1 HG00597.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1319+2918_1319+292 others(14): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12632083 | ||||||
chr7:12632083 | C | CATTTTAT others(8): Show |
12 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0002g0095 others(9): Show |
12 | HG01106.hp2 HG01175.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1319+2913_1319+292 others(19): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12632083 | ||||||
chr7:12632083 | C | CATTTTAT others(13): Show |
4 | a0001c0001t0002g0087 a0001c0001t0009g0209 a0001c0001t0115g0100 others(1): Show |
4 | HG02129.hp2 NA18959.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.1319+2908_1319+292 others(24): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12632083 | ||||||
chr7:12632083 | C | CATTTTAT others(23): Show |
3 | a0001c0001t0005g0139 a0001c0001t0005g0158 a0001c0001t0073g0036 |
3 | HG01515.hp1 HG01517.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1319+2898_1319+292 others(34): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12632083 | ||||||
chr7:12632083 | CATTTT | C | 32 | a0001c0001t0003g0181 a0001c0001t0003g0193 a0001c0001t0003g0217 others(29): Show |
33 | HG00735.hp1 HG01069.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1319+2923_1319+292 others(9): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12632083 | ||||||
chr7:12632083 | CATTTTAT others(3): Show |
C | 25 | a0001c0001t0001g0026 a0001c0001t0001g0079 a0001c0001t0001g0088 others(22): Show |
27 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1319+2918_1319+292 others(14): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12632083 | ||||||
chr7:12632083 | CATTTTAT others(8): Show |
C | 84 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0121 others(81): Show |
84 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1319+2913_1319+292 others(19): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12632083 | ||||||
chr7:12632083 | CATTTTAT others(13): Show |
C | 25 | a0001c0001t0121g0201 a0001c0001t0124g0185 a0002c0002t0001g0276 others(22): Show |
26 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319+2908_1319+292 others(24): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12632083 | ||||||
chr7:12632083 | CATTTTAT others(18): Show |
C | 3 | a0001c0001t0016g0023 a0001c0001t0092g0141 a0002c0002t0008g0058 |
3 | HG02602.hp2 NA19057.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1319+2903_1319+292 others(29): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12632083 | ||||||
chr7:12632114 | A | ATTTTATT others(1): Show |
6 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1319+2894_1319+290 others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12632114 | ||||||
chr7:12632139 | A | AATTTTAT others(6): Show |
6 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1319+2917_1319+291 others(17): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12632139 | |||||||
chr7:12632217 | G | A | 1 | a0001c0001t0050g0349 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1319+2995G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12632217 | |||||||
chr7:12632255 | C | T | 75 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(72): Show |
79 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1319+3033C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12632255 | |||||||
chr7:12632415 | G | A | 1 | a0001c0001t0162g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1319+3193G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12632415 | |||||||
chr7:12632428 | G | C | 101 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(98): Show |
101 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1319+3206G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12632428 | |||||||
chr7:12632823 | C | T | 6 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1320-3222C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12632823 | |||||||
chr7:12633131 | C | G | 1 | a0004c0005t0006g0221 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1320-2914C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12633131 | |||||||
chr7:12633140 | G | A | 1 | a0001c0001t0086g0107 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1320-2905G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12633140 | |||||||
chr7:12633207 | G | T | 94 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(91): Show |
98 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1320-2838G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12633207 | |||||||
chr7:12633245 | A | C | 107 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(104): Show |
107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1320-2800A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12633245 | |||||||
chr7:12633436 | G | A | 1 | a0001c0001t0023g0140 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1320-2609G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12633436 | |||||||
chr7:12633732 | C | T | 5 | a0005c0007t0006g0335 a0005c0007t0034g0350 a0005c0007t0047g0338 others(2): Show |
6 | HG02145.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1320-2313C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12633732 | |||||||
chr7:12633839 | C | T | 10 | a0004c0005t0006g0221 a0004c0005t0014g0202 a0004c0005t0019g0177 others(7): Show |
10 | HG00738.hp1 HG00741.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1320-2206C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12633839 | |||||||
chr7:12633959 | G | A | 107 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(104): Show |
112 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1320-2086G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12633959 | |||||||
chr7:12633965 | G | GT | 47 | a0001c0001t0001g0055 a0001c0001t0001g0146 a0001c0001t0003g0182 others(44): Show |
48 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.1320-2066dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12633965 | ||||||
chr7:12633965 | GT | G | 93 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(90): Show |
98 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1320-2066delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12633965 | ||||||
chr7:12634059 | C | A | 1 | a0004c0005t0006g0221 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1320-1986C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634059 | |||||||
chr7:12634080 | G | A | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1320-1965G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634080 | |||||||
chr7:12634312 | C | A | 1 | a0002c0002t0001g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1320-1733C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634312 | |||||||
chr7:12634342 | G | A | 8 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0003t0006g0337 others(5): Show |
9 | HG00099.hp1 HG01433.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1320-1703G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634342 | |||||||
chr7:12634459 | T | C | 1 | a0008c0009t0006g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1320-1586T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634459 | |||||||
chr7:12634486 | CA | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(220): Show |
228 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.1320-1544delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12634486 | ||||||
chr7:12634520 | A | G | 1 | a0001c0001t0003g0078 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1320-1525A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634520 | |||||||
chr7:12634576 | T | C | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1320-1469T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634576 | |||||||
chr7:12634606 | G | T | 3 | a0009c0012t0080g0283 a0009c0012t0082g0284 a0009c0012t0085g0282 |
3 | HG02257.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1320-1439G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634606 | |||||||
chr7:12634740 | C | T | 4 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0002c0014t0006g0060 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1320-1305C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634740 | |||||||
chr7:12634775 | A | G | 1 | a0002c0002t0001g0304 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1320-1270A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634775 | |||||||
chr7:12634897 | T | C | 10 | a0004c0005t0006g0221 a0004c0005t0014g0202 a0004c0005t0019g0177 others(7): Show |
10 | HG00738.hp1 HG00741.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1320-1148T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634897 | |||||||
chr7:12634922 | C | T | 112 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(109): Show |
117 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1320-1123C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634922 | |||||||
chr7:12634953 | G | A | 26 | a0001c0001t0001g0079 a0001c0001t0001g0124 a0001c0001t0001g0125 others(23): Show |
26 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1320-1092G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12634953 | |||||||
chr7:12635016 | G | A | 112 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(109): Show |
117 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1320-1029G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635016 | |||||||
chr7:12635156 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1320-889G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635156 | |||||||
chr7:12635378 | G | A | 1 | a0001c0001t0116g0136 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1320-667G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635378 | |||||||
chr7:12635416 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1320-629C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635416 | |||||||
chr7:12635461 | A | T | 10 | a0004c0005t0006g0221 a0004c0005t0014g0202 a0004c0005t0019g0177 others(7): Show |
10 | HG00738.hp1 HG00741.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1320-584A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635461 | |||||||
chr7:12635470 | G | A | 1 | a0001c0001t0145g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1320-575G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635470 | |||||||
chr7:12635537 | G | A | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1320-508G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635537 | |||||||
chr7:12635600 | G | A | 328 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(325): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1320-445G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635600 | |||||||
chr7:12635607 | G | A | 1 | a0002c0003t0022g0248 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1320-438G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635607 | |||||||
chr7:12635611 | C | CA | 37 | a0001c0001t0001g0055 a0001c0001t0003g0054 a0001c0001t0003g0206 others(34): Show |
37 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1320-403dupA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635611 | C | CAA | 36 | a0001c0001t0003g0182 a0001c0001t0013g0163 a0001c0001t0022g0174 others(33): Show |
37 | HG00099.hp2 HG00140.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1320-404_1320-403d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635611 | C | CAAA | 12 | a0001c0001t0013g0020 a0001c0001t0030g0194 a0001c0001t0040g0225 others(9): Show |
12 | HG00642.hp1 HG01070.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1320-405_1320-403d others(5): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635611 | C | CAAAA | 6 | a0001c0001t0001g0146 a0001c0001t0030g0115 a0001c0001t0145g0041 others(3): Show |
6 | HG00735.hp2 HG01168.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1320-406_1320-403d others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635611 | C | CAAAAA | 16 | a0001c0001t0002g0145 a0001c0001t0007g0051 a0001c0001t0011g0046 others(13): Show |
16 | HG01175.hp2 HG01993.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.1320-407_1320-403d others(7): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635611 | C | CAAAAAA | 8 | a0001c0001t0001g0029 a0001c0001t0021g0010 a0001c0001t0028g0047 others(5): Show |
8 | HG00438.hp1 HG02027.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1320-408_1320-403d others(8): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635611 | C | CAAAAAAA | 18 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0005g0144 others(15): Show |
18 | HG01106.hp1 HG01109.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.1320-409_1320-403d others(9): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635611 | C | CAAAAAAA others(1): Show |
24 | a0001c0001t0001g0088 a0001c0001t0001g0121 a0001c0001t0002g0170 others(21): Show |
24 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.1320-410_1320-403d others(10): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635611 | C | CAAAAAAA others(3): Show |
12 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0214 others(9): Show |
12 | HG00621.hp1 HG02071.hp2 NA18971.hp1 others(9): Show |
intron_variant | MODIFIER | c.1320-412_1320-403d others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635611 | C | CAAAAAAA others(4): Show |
14 | a0001c0001t0001g0079 a0001c0001t0001g0125 a0001c0001t0005g0094 others(11): Show |
14 | HG00423.hp1 HG00558.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1320-413_1320-403d others(13): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635611 | CA | C | 28 | a0001c0001t0006g0016 a0001c0001t0014g0021 a0001c0001t0020g0196 others(25): Show |
29 | HG00741.hp2 HG01168.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1320-403delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635611 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0024g0099 a0010c0011t0135g0353 |
2 | HG02040.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1320-412_1320-403d others(12): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635611 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0162g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1320-413_1320-403d others(13): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 12635611 | ||||||
chr7:12635653 | A | G | 17 | a0001c0001t0001g0055 a0001c0001t0003g0119 a0001c0001t0045g0211 others(14): Show |
17 | HG00597.hp2 HG00673.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1320-392A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635653 | |||||||
chr7:12635744 | G | A | 274 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1320-301G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635744 | |||||||
chr7:12635757 | A | G | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1320-288A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635757 | |||||||
chr7:12635786 | G | A | 1 | a0001c0001t0083g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1320-259G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635786 | |||||||
chr7:12635804 | C | A | 2 | a0001c0001t0107g0097 a0001c0001t0120g0075 |
2 | NA19010.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1320-241C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635804 | |||||||
chr7:12635921 | A | G | 100 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(97): Show |
100 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1320-124A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12635921 | |||||||
chr7:12636024 | G | A | 5 | a0004c0005t0019g0177 a0004c0005t0049g0346 a0004c0005t0104g0138 others(2): Show |
5 | HG00738.hp1 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1320-21G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12636024 | |||||||
chr7:12636024 | G | T | 1 | a0001c0001t0101g0122 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1320-21G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 9/15 | chr7 | 12636024 | |||||||
chr7:12636562 | C | T | 100 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(97): Show |
100 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1410+427C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12636562 | |||||||
chr7:12636603 | A | G | 10 | a0004c0005t0006g0221 a0004c0005t0014g0202 a0004c0005t0019g0177 others(7): Show |
10 | HG00738.hp1 HG00741.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1410+468A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12636603 | |||||||
chr7:12636678 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1410+543A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12636678 | |||||||
chr7:12636724 | A | G | 1 | a0001c0001t0164g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1410+589A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12636724 | |||||||
chr7:12636779 | G | A | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1410+644G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12636779 | |||||||
chr7:12636836 | C | G | 1 | a0001c0001t0023g0162 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1410+701C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12636836 | |||||||
chr7:12636919 | T | TA | 100 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(97): Show |
100 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1410+793dupA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 12636919 | ||||||
chr7:12637013 | C | G | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1410+878C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12637013 | |||||||
chr7:12637068 | G | A | 1 | a0010c0011t0135g0353 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1410+933G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12637068 | |||||||
chr7:12637247 | G | A | 1 | a0002c0002t0001g0258 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1410+1112G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12637247 | |||||||
chr7:12637270 | G | A | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1410+1135G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12637270 | |||||||
chr7:12637270 | G | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(87): Show |
94 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.1410+1135G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12637270 | |||||||
chr7:12637303 | G | A | 100 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(97): Show |
100 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1410+1168G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12637303 | |||||||
chr7:12637669 | T | C | 202 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(199): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1410+1534T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12637669 | |||||||
chr7:12637845 | C | G | 75 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(72): Show |
79 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1410+1710C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12637845 | |||||||
chr7:12637856 | T | TAG | 75 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(72): Show |
79 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1410+1725_1410+172 others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 12637856 | ||||||
chr7:12637862 | C | CAG | 231 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(228): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1410+1729_1410+173 others(6): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 12637862 | ||||||
chr7:12637862 | C | G | 75 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(72): Show |
79 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1410+1727C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12637862 | |||||||
chr7:12637948 | G | A | 202 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(199): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1410+1813G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12637948 | |||||||
chr7:12638006 | C | G | 55 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(52): Show |
55 | HG00544.hp2 HG00597.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.1410+1871C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638006 | |||||||
chr7:12638076 | A | G | 7 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1410+1941A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638076 | |||||||
chr7:12638089 | C | T | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1410+1954C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638089 | |||||||
chr7:12638220 | G | A | 100 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(97): Show |
100 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1410+2085G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638220 | |||||||
chr7:12638244 | C | G | 77 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0091 others(74): Show |
81 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1411-2103C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638244 | |||||||
chr7:12638320 | C | A | 1 | a0002c0002t0031g0285 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1411-2027C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638320 | |||||||
chr7:12638386 | C | T | 2 | a0002c0003t0015g0065 a0002c0003t0146g0062 |
2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1411-1961C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638386 | |||||||
chr7:12638591 | C | A | 2 | a0002c0002t0129g0007 a0002c0002t0130g0007 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1411-1756C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638591 | |||||||
chr7:12638654 | C | T | 15 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1411-1693C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638654 | |||||||
chr7:12638663 | A | G | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1411-1684A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638663 | |||||||
chr7:12638725 | C | G | 1 | a0002c0003t0010g0287 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1411-1622C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638725 | |||||||
chr7:12638745 | T | G | 202 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(199): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1411-1602T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638745 | |||||||
chr7:12638928 | T | C | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1411-1419T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12638928 | |||||||
chr7:12639107 | C | T | 28 | a0001c0001t0001g0055 a0001c0001t0003g0119 a0001c0001t0006g0016 others(25): Show |
28 | HG00597.hp2 HG00673.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.1411-1240C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12639107 | |||||||
chr7:12639257 | A | G | 15 | a0001c0001t0014g0112 a0001c0001t0017g0220 a0001c0001t0020g0113 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1411-1090A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12639257 | |||||||
chr7:12639522 | A | G | 5 | a0001c0001t0093g0043 a0002c0002t0020g0246 a0002c0003t0015g0340 others(2): Show |
5 | HG02055.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411-825A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12639522 | |||||||
chr7:12639786 | C | T | 1 | a0001c0001t0008g0096 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1411-561C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12639786 | |||||||
chr7:12639863 | T | G | 1 | a0008c0009t0110g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1411-484T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12639863 | |||||||
chr7:12640009 | T | G | 49 | a0001c0001t0001g0159 a0001c0001t0002g0095 a0001c0001t0003g0054 others(46): Show |
49 | HG00544.hp2 HG00597.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.1411-338T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12640009 | |||||||
chr7:12640080 | A | G | 1 | a0001c0001t0003g0078 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1411-267A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12640080 | |||||||
chr7:12640086 | A | G | 2 | a0002c0014t0006g0060 a0002c0014t0184g0059 |
2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1411-261A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12640086 | |||||||
chr7:12640137 | C | A | 112 | a0001c0001t0001g0146 a0001c0001t0001g0159 a0001c0001t0002g0095 others(109): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1411-210C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12640137 | |||||||
chr7:12640268 | T | C | 1 | a0001c0001t0020g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1411-79T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 10/15 | chr7 | 12640268 | |||||||
chr7:12640607 | G | A | 6 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(3): Show |
6 | HG02970.hp2 HG02976.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1581+90G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12640607 | |||||||
chr7:12640829 | A | G | 103 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(100): Show |
104 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1581+312A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12640829 | |||||||
chr7:12640889 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1581+372C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12640889 | |||||||
chr7:12641071 | T | G | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1581+554T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12641071 | |||||||
chr7:12641093 | A | G | 2 | a0002c0002t0129g0007 a0002c0002t0130g0007 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1581+576A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12641093 | |||||||
chr7:12641289 | C | T | 2 | a0002c0014t0006g0060 a0002c0014t0184g0059 |
2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1581+772C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12641289 | |||||||
chr7:12641290 | A | G | 1 | a0002c0002t0020g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1581+773A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12641290 | |||||||
chr7:12641371 | A | G | 1 | a0002c0002t0008g0058 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1581+854A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12641371 | |||||||
chr7:12641385 | C | T | 3 | a0002c0002t0002g0310 a0002c0003t0010g0287 a0012c0018t0002g0302 |
3 | HG00140.hp1 HG01433.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1581+868C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12641385 | |||||||
chr7:12641471 | G | C | 213 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(210): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1581+954G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12641471 | |||||||
chr7:12641563 | C | T | 4 | a0004c0005t0006g0221 a0004c0005t0014g0202 a0004c0005t0042g0116 others(1): Show |
4 | HG00741.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1581+1046C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12641563 | |||||||
chr7:12641597 | G | A | 7 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(4): Show |
7 | HG02970.hp2 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1581+1080G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12641597 | |||||||
chr7:12641606 | C | T | 1 | a0001c0001t0051g0347 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1581+1089C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12641606 | |||||||
chr7:12641614 | C | T | 2 | a0001c0001t0074g0052 a0001c0001t0075g0179 |
2 | NA18939.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.1581+1097C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12641614 | |||||||
chr7:12641897 | T | A | 219 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1581+1380T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12641897 | |||||||
chr7:12642469 | G | A | 1 | a0001c0001t0007g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1582-1669G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12642469 | |||||||
chr7:12642493 | G | A | 1 | a0001c0001t0008g0096 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1582-1645G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12642493 | |||||||
chr7:12642689 | A | G | 5 | a0001c0001t0001g0091 a0001c0001t0107g0097 a0001c0001t0116g0136 others(2): Show |
5 | NA18945.hp2 NA18970.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1582-1449A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12642689 | |||||||
chr7:12642860 | G | T | 1 | a0001c0001t0005g0208 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1582-1278G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12642860 | |||||||
chr7:12642908 | A | G | 3 | a0001c0001t0003g0037 a0001c0001t0095g0039 a0001c0001t0163g0035 |
3 | HG03831.hp2 NA18943.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1582-1230A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12642908 | |||||||
chr7:12642925 | A | G | 4 | a0001c0001t0003g0181 a0001c0001t0003g0192 a0001c0001t0003g0193 others(1): Show |
4 | NA19010.hp1 NA19011.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1582-1213A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12642925 | |||||||
chr7:12642992 | T | A | 1 | a0002c0014t0184g0059 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1582-1146T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12642992 | |||||||
chr7:12643031 | A | G | 1 | a0002c0002t0113g0277 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1582-1107A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643031 | |||||||
chr7:12643240 | T | A | 55 | a0001c0001t0001g0146 a0001c0001t0003g0182 a0001c0001t0013g0020 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1582-898T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643240 | |||||||
chr7:12643276 | A | G | 1 | a0001c0001t0016g0023 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1582-862A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643276 | |||||||
chr7:12643294 | A | G | 114 | a0001c0001t0001g0146 a0001c0001t0001g0159 a0001c0001t0002g0095 others(111): Show |
115 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1582-844A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643294 | |||||||
chr7:12643320 | C | G | 97 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(94): Show |
97 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1582-818C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643320 | |||||||
chr7:12643386 | A | T | 97 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(94): Show |
97 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1582-752A>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643386 | |||||||
chr7:12643392 | G | A | 305 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(302): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1582-746G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643392 | |||||||
chr7:12643514 | T | C | 97 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(94): Show |
97 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1582-624T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643514 | |||||||
chr7:12643573 | T | C | 1 | a0001c0001t0066g0045 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1582-565T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643573 | |||||||
chr7:12643753 | T | C | 2 | a0001c0001t0136g0117 a0002c0014t0006g0060 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1582-385T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643753 | |||||||
chr7:12643756 | C | T | 1 | a0002c0002t0026g0352 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1582-382C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643756 | |||||||
chr7:12643821 | C | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0101 others(36): Show |
40 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.1582-317C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643821 | |||||||
chr7:12643979 | T | G | 98 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(95): Show |
99 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1582-159T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12643979 | |||||||
chr7:12644012 | G | A | 1 | a0002c0003t0006g0337 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1582-126G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12644012 | |||||||
chr7:12644031 | G | A | 55 | a0001c0001t0001g0146 a0001c0001t0003g0182 a0001c0001t0013g0020 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1582-107G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 11/15 | chr7 | 12644031 | |||||||
chr7:12644375 | T | C | 1 | a0001c0001t0083g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1759+60T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 12/15 | chr7 | 12644375 | |||||||
chr7:12644385 | A | G | 32 | a0001c0001t0001g0048 a0001c0001t0001g0143 a0001c0001t0003g0181 others(29): Show |
35 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1759+70A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 12/15 | chr7 | 12644385 | |||||||
chr7:12644528 | G | A | 1 | a0002c0014t0184g0059 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1760-56G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 12/15 | chr7 | 12644528 | |||||||
chr7:12644715 | C | T | 308 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(305): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1881+10C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12644715 | |||||||
chr7:12645018 | T | TA | 176 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(173): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1881+331dupA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 12645018 | ||||||
chr7:12645018 | T | TAA | 64 | a0001c0001t0001g0055 a0001c0001t0003g0119 a0001c0001t0005g0229 others(61): Show |
64 | HG00597.hp2 HG00673.hp1 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.1881+330_1881+331d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 12645018 | ||||||
chr7:12645018 | TA | T | 14 | a0001c0001t0179g0014 a0002c0002t0001g0252 a0003c0004t0002g0149 others(11): Show |
14 | HG00099.hp1 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1881+331delA | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 12645018 | ||||||
chr7:12645041 | C | T | 18 | a0001c0001t0020g0196 a0001c0001t0042g0195 a0001c0001t0164g0197 others(15): Show |
19 | HG00099.hp1 HG01433.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1881+336C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645041 | |||||||
chr7:12645048 | G | A | 1 | a0001c0001t0054g0345 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1881+343G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645048 | |||||||
chr7:12645189 | G | A | 22 | a0001c0001t0001g0029 a0001c0001t0002g0092 a0001c0001t0002g0145 others(19): Show |
22 | HG00408.hp1 HG00438.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1881+484G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645189 | |||||||
chr7:12645230 | A | C | 1 | a0001c0001t0055g0348 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1881+525A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645230 | |||||||
chr7:12645376 | C | T | 162 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(159): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1881+671C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645376 | |||||||
chr7:12645417 | G | A | 25 | a0001c0001t0014g0112 a0001c0001t0037g0012 a0001c0001t0042g0195 others(22): Show |
25 | HG00099.hp1 HG00741.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1881+712G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645417 | |||||||
chr7:12645491 | T | C | 1 | a0001c0001t0133g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1881+786T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645491 | |||||||
chr7:12645561 | A | G | 278 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(275): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1881+856A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645561 | |||||||
chr7:12645608 | C | G | 41 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0091 others(38): Show |
43 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.1881+903C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645608 | |||||||
chr7:12645630 | G | A | 6 | a0006c0006t0007g0151 a0006c0006t0011g0152 a0006c0006t0018g0176 others(3): Show |
6 | NA18940.hp1 NA18945.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1881+925G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645630 | |||||||
chr7:12645647 | T | C | 10 | a0001c0001t0006g0016 a0001c0001t0050g0349 a0001c0001t0133g0198 others(7): Show |
10 | HG02280.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1881+942T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645647 | |||||||
chr7:12645868 | C | T | 2 | a0001c0001t0043g0227 a0001c0001t0043g0228 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1881+1163C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645868 | |||||||
chr7:12645891 | A | G | 265 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(262): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1881+1186A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645891 | |||||||
chr7:12645905 | G | A | 101 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(98): Show |
101 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1881+1200G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645905 | |||||||
chr7:12645963 | G | T | 1 | a0002c0014t0184g0059 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1881+1258G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12645963 | |||||||
chr7:12646075 | A | G | 13 | a0001c0001t0014g0021 a0001c0001t0020g0196 a0001c0001t0121g0201 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1881+1370A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12646075 | |||||||
chr7:12646088 | T | C | 1 | a0001c0001t0020g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1881+1383T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12646088 | |||||||
chr7:12646125 | T | C | 12 | a0001c0001t0014g0112 a0001c0001t0027g0013 a0001c0001t0027g0042 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.1881+1420T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12646125 | |||||||
chr7:12646356 | C | A | 3 | a0001c0001t0071g0022 a0002c0002t0005g0319 a0002c0002t0078g0321 |
3 | HG01192.hp2 HG02300.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1881+1651C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12646356 | |||||||
chr7:12646382 | G | A | 2 | a0002c0003t0015g0065 a0002c0019t0064g0354 |
2 | HG01255.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1881+1677G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12646382 | |||||||
chr7:12646382 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1881+1677G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12646382 | |||||||
chr7:12646400 | G | T | 1 | a0002c0002t0168g0316 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1881+1695G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12646400 | |||||||
chr7:12646523 | G | A | 3 | a0002c0003t0015g0340 a0010c0011t0031g0005 a0010c0011t0111g0005 |
3 | HG02896.hp2 HG02897.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1881+1818G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12646523 | |||||||
chr7:12646540 | A | G | 1 | a0001c0001t0095g0039 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1881+1835A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12646540 | |||||||
chr7:12646569 | A | G | 153 | a0001c0001t0001g0146 a0001c0001t0003g0037 a0001c0001t0003g0181 others(150): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1881+1864A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12646569 | |||||||
chr7:12646646 | G | A | 141 | a0001c0001t0001g0146 a0001c0001t0003g0037 a0001c0001t0003g0181 others(138): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1881+1941G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12646646 | |||||||
chr7:12646937 | G | C | 1 | a0002c0002t0001g0276 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1881+2232G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12646937 | |||||||
chr7:12647019 | G | GACTGGTA | 85 | a0001c0001t0001g0146 a0001c0001t0003g0037 a0001c0001t0003g0182 others(82): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1881+2317_1881+231 others(11): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 12647019 | ||||||
chr7:12647092 | A | G | 1 | a0001c0001t0141g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1882-2375A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12647092 | |||||||
chr7:12647190 | G | T | 8 | a0001c0001t0017g0220 a0001c0001t0042g0195 a0001c0001t0164g0197 others(5): Show |
8 | HG00741.hp2 HG02258.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1882-2277G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12647190 | |||||||
chr7:12647349 | AT | A | 3 | a0001c0001t0001g0146 a0002c0002t0010g0317 a0002c0002t0077g0314 |
3 | HG00735.hp2 HG02145.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1882-2116delT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 12647349 | ||||||
chr7:12647350 | T | A | 1 | a0001c0001t0006g0016 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1882-2117T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12647350 | |||||||
chr7:12647460 | G | A | 5 | a0002c0002t0031g0285 a0002c0003t0015g0065 a0002c0003t0017g0066 others(2): Show |
5 | HG01243.hp1 HG01255.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1882-2007G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12647460 | |||||||
chr7:12647503 | G | C | 2 | a0001c0001t0043g0227 a0001c0001t0043g0228 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1882-1964G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12647503 | |||||||
chr7:12647752 | A | C | 5 | a0001c0001t0019g0224 a0001c0001t0179g0014 a0002c0002t0001g0252 others(2): Show |
5 | HG00099.hp1 HG01255.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1882-1715A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12647752 | |||||||
chr7:12647854 | C | T | 7 | a0001c0001t0005g0212 a0001c0001t0095g0039 a0002c0002t0004g0273 others(4): Show |
7 | HG01346.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.1882-1613C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12647854 | |||||||
chr7:12648028 | C | T | 6 | a0001c0001t0017g0220 a0001c0001t0042g0195 a0001c0001t0164g0197 others(3): Show |
6 | HG00741.hp2 HG02622.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1882-1439C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648028 | |||||||
chr7:12648038 | G | C | 1 | a0001c0001t0011g0034 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1882-1429G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648038 | |||||||
chr7:12648146 | C | A | 58 | a0001c0001t0001g0146 a0001c0001t0003g0037 a0001c0001t0003g0182 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1882-1321C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648146 | |||||||
chr7:12648146 | C | G | 2 | a0001c0001t0179g0014 a0002c0002t0001g0252 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1882-1321C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648146 | |||||||
chr7:12648162 | A | C | 1 | a0001c0001t0141g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1882-1305A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648162 | |||||||
chr7:12648246 | T | C | 5 | a0001c0001t0019g0224 a0001c0001t0179g0014 a0002c0002t0001g0252 others(2): Show |
5 | HG00099.hp1 HG01255.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1882-1221T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648246 | |||||||
chr7:12648295 | C | CT | 60 | a0001c0001t0001g0146 a0001c0001t0003g0037 a0001c0001t0003g0182 others(57): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1882-1155dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 12648295 | ||||||
chr7:12648319 | C | T | 1 | a0001c0001t0141g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1882-1148C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648319 | |||||||
chr7:12648320 | G | A | 13 | a0001c0001t0006g0016 a0001c0001t0020g0196 a0001c0001t0121g0201 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1882-1147G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648320 | |||||||
chr7:12648587 | G | A | 12 | a0001c0001t0014g0112 a0001c0001t0027g0013 a0001c0001t0027g0042 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.1882-880G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648587 | |||||||
chr7:12648752 | G | A | 3 | a0001c0001t0020g0113 a0001c0001t0133g0198 a0002c0003t0143g0232 |
3 | HG02622.hp2 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1882-715G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648752 | |||||||
chr7:12648817 | A | G | 3 | a0004c0005t0049g0346 a0004c0005t0106g0184 a0011c0013t0009g0257 |
3 | HG01975.hp1 HG01978.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1882-650A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648817 | |||||||
chr7:12648846 | G | A | 1 | a0002c0003t0036g0006 | 2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1882-621G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648846 | |||||||
chr7:12648900 | G | A | 1 | a0002c0003t0089g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1882-567G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648900 | |||||||
chr7:12648906 | G | A | 13 | a0001c0001t0017g0220 a0001c0001t0042g0195 a0001c0001t0164g0197 others(10): Show |
13 | HG00741.hp2 HG01243.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1882-561G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12648906 | |||||||
chr7:12649068 | A | C | 363 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(360): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1882-399A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12649068 | |||||||
chr7:12649101 | C | T | 12 | a0001c0001t0014g0112 a0001c0001t0027g0013 a0001c0001t0027g0042 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.1882-366C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 13/15 | chr7 | 12649101 | |||||||
chr7:12649547 | A | G | 2 | a0001c0001t0023g0162 a0001c0001t0152g0161 |
2 | HG02155.hp1 NA18946.hp2 |
splice_region_variant&intron_variant | LOW | c.1959+3A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12649547 | |||||||
chr7:12649560 | G | A | 1 | a0002c0002t0002g0330 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1959+16G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12649560 | |||||||
chr7:12649697 | C | T | 5 | a0001c0001t0019g0224 a0001c0001t0179g0014 a0002c0002t0001g0252 others(2): Show |
5 | HG00099.hp1 HG01255.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1959+153C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12649697 | |||||||
chr7:12649833 | T | A | 11 | a0001c0001t0017g0220 a0001c0001t0042g0195 a0001c0001t0164g0197 others(8): Show |
11 | HG00741.hp2 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1959+289T>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12649833 | |||||||
chr7:12649850 | G | T | 123 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0055 others(120): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1959+306G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12649850 | |||||||
chr7:12649860 | G | A | 4 | a0001c0001t0013g0020 a0002c0002t0002g0322 a0002c0002t0041g0325 others(1): Show |
4 | HG00642.hp1 HG01243.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1959+316G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12649860 | |||||||
chr7:12649910 | G | A | 1 | a0001c0001t0124g0185 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1959+366G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12649910 | |||||||
chr7:12649989 | C | T | 25 | a0001c0001t0003g0181 a0001c0001t0003g0192 a0001c0001t0003g0193 others(22): Show |
28 | HG00735.hp1 HG01069.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1959+445C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12649989 | |||||||
chr7:12649992 | T | G | 3 | a0001c0001t0022g0174 a0001c0001t0022g0175 a0002c0002t0001g0304 |
3 | HG03490.hp1 HG03492.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1959+448T>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12649992 | |||||||
chr7:12650124 | A | C | 1 | a0002c0002t0012g0303 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1959+580A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12650124 | |||||||
chr7:12650401 | A | G | 27 | a0001c0001t0003g0181 a0001c0001t0003g0192 a0001c0001t0003g0193 others(24): Show |
30 | HG00735.hp1 HG01069.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1959+857A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12650401 | |||||||
chr7:12650476 | T | C | 4 | a0002c0002t0031g0285 a0002c0002t0180g0245 a0002c0003t0017g0066 others(1): Show |
4 | HG01243.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1959+932T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12650476 | |||||||
chr7:12650541 | G | C | 1 | a0002c0002t0001g0304 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1959+997G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12650541 | |||||||
chr7:12650578 | A | G | 2 | a0001c0001t0003g0002 a0001c0001t0010g0167 |
3 | HG01069.hp2 HG01071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1959+1034A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12650578 | |||||||
chr7:12650770 | A | C | 1 | a0001c0001t0181g0017 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1960-1071A>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12650770 | |||||||
chr7:12650793 | G | T | 85 | a0001c0001t0003g0181 a0001c0001t0003g0192 a0001c0001t0003g0193 others(82): Show |
89 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(86): Show |
intron_variant | MODIFIER | c.1960-1048G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12650793 | |||||||
chr7:12650811 | G | A | 3 | a0002c0003t0006g0234 a0002c0003t0017g0231 a0002c0003t0017g0233 |
3 | HG02257.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1960-1030G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12650811 | |||||||
chr7:12650875 | G | A | 1 | a0001c0001t0124g0185 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1960-966G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12650875 | |||||||
chr7:12650989 | C | A | 9 | a0001c0001t0006g0016 a0001c0001t0017g0220 a0001c0001t0020g0196 others(6): Show |
9 | HG02257.hp1 HG02622.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1960-852C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12650989 | |||||||
chr7:12651204 | G | C | 1 | a0001c0001t0132g0186 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1960-637G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12651204 | |||||||
chr7:12651507 | C | G | 80 | a0001c0001t0002g0095 a0001c0001t0003g0181 a0001c0001t0003g0191 others(77): Show |
83 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1960-334C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | chr7 | 12651507 | |||||||
chr7:12651549 | G | GT | 74 | a0001c0001t0001g0121 a0001c0001t0002g0095 a0001c0001t0003g0181 others(71): Show |
76 | HG00544.hp2 HG00642.hp1 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.1960-283dupT | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr7 | 12651549 | ||||||
chr7:12651937 | G | A | 1 | a0002c0003t0010g0287 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2020+36G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | chr7 | 12651937 | |||||||
chr7:12651953 | G | A | 1 | a0001c0001t0183g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2020+52G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | chr7 | 12651953 | |||||||
chr7:12652078 | G | C | 89 | a0001c0001t0001g0004 a0001c0001t0003g0002 a0001c0001t0003g0037 others(86): Show |
93 | HG00544.hp2 HG01069.hp1 HG01069.hp2 others(90): Show |
intron_variant | MODIFIER | c.2020+177G>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | chr7 | 12652078 | |||||||
chr7:12652143 | A | G | 1 | a0002c0002t0077g0314 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2020+242A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | chr7 | 12652143 | |||||||
chr7:12652243 | T | C | 74 | a0001c0001t0002g0087 a0001c0001t0002g0092 a0001c0001t0002g0093 others(71): Show |
75 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.2020+342T>C | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | chr7 | 12652243 | |||||||
chr7:12652314 | G | T | 207 | a0001c0001t0001g0026 a0001c0001t0001g0048 a0001c0001t0001g0055 others(204): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.2021-274G>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | chr7 | 12652314 | |||||||
chr7:12652343 | A | ATG | 74 | a0001c0001t0002g0087 a0001c0001t0002g0092 a0001c0001t0002g0093 others(71): Show |
75 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.2021-243_2021-242d others(4): Show |
SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr7 | 12652343 | ||||||
chr7:12652363 | C | T | 169 | a0001c0001t0002g0087 a0001c0001t0002g0092 a0001c0001t0002g0093 others(166): Show |
175 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.2021-225C>T | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | chr7 | 12652363 | |||||||
chr7:12652441 | G | A | 1 | a0001c0001t0009g0180 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2021-147G>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | chr7 | 12652441 | |||||||
chr7:12652459 | A | G | 1 | a0002c0003t0161g0067 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2021-129A>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | chr7 | 12652459 | |||||||
chr7:12652465 | C | G | 1 | a0001c0001t0136g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2021-123C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | chr7 | 12652465 | |||||||
chr7:12652481 | C | G | 81 | a0001c0001t0003g0002 a0001c0001t0003g0037 a0001c0001t0003g0054 others(78): Show |
85 | HG00544.hp2 HG01069.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.2021-107C>G | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | chr7 | 12652481 | |||||||
chr7:12652535 | C | A | 1 | a0001c0001t0132g0186 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2021-53C>A | SCIN | ENSG00000006747.15 | transcript | ENST00000297029.10 | protein_coding | 15/15 | chr7 | 12652535 |