Item | Value |
---|---|
geneid | 9671 |
ensemblid | ENSG00000075035.10 |
hgncid | 29117 |
symbol | WSCD2 |
name | WSC domain containing 2 |
refseq_nuc | NM_014653.4 |
refseq_prot | NP_055468.2 |
ensembl_nuc | ENST00000547525.6 |
ensembl_prot | ENSP00000448047.1 |
mane_status | MANE Select |
chr | chr12 |
start | 108129288 |
end | 108250537 |
strand | + |
ver | v1.2 |
region | chr12:108129288-108250537 |
region5000 | chr12:108124288-108255537 |
regionname0 | WSCD2_chr12_108129288_108250537 |
regionname5000 | WSCD2_chr12_108124288_108255537 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 565 | 229 | 84 | 50 | 56 | 13 | 25 | 40 | WSCD2_chr12_108124288_108255537 | WSCD2 | MAKLW others(560): Show |
chr12 | 108124288 | 108255537 |
a0002 | 0/1 | 565 | 47 | 2 | 11 | 25 | 1 | 7 | 18 | WSCD2_chr12_108124288_108255537 | WSCD2 | MAKLW others(560): Show |
chr12 | 108124288 | 108255537 |
a0003 | 0/0 | 565 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | MAKLW others(560): Show |
chr12 | 108124288 | 108255537 |
a0004 | 0/0 | 565 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | MAKLW others(560): Show |
chr12 | 108124288 | 108255537 |
a0005 | 0/0 | 565 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | MAKLW others(560): Show |
chr12 | 108124288 | 108255537 |
a0006 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | MAKLW others(560): Show |
chr12 | 108124288 | 108255537 |
a0007 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | MAKLW others(560): Show |
chr12 | 108124288 | 108255537 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1695 | 220 | 78 | 48 | 55 | 13 | 25 | WSCD2_chr12_108124288_108255537 | WSCD2 | ATGGC others(1690): Show |
chr12 | 108124288 | 108255537 | ||
a0001c0003 | 0/0 | 1695 | 7 | 6 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | ATGGC others(1690): Show |
chr12 | 108124288 | 108255537 | ||
a0001c0008 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | ATGGC others(1690): Show |
chr12 | 108124288 | 108255537 | ||
a0001c0010 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | ATGGC others(1690): Show |
chr12 | 108124288 | 108255537 | ||
a0002c0002 | 0/1 | 1695 | 46 | 2 | 11 | 24 | 1 | 7 | WSCD2_chr12_108124288_108255537 | WSCD2 | ATGGC others(1690): Show |
chr12 | 108124288 | 108255537 | ||
a0002c0009 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | ATGGC others(1690): Show |
chr12 | 108124288 | 108255537 | ||
a0003c0004 | 0/0 | 1695 | 4 | 4 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | ATGGC others(1690): Show |
chr12 | 108124288 | 108255537 | ||
a0004c0007 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | ATGGC others(1690): Show |
chr12 | 108124288 | 108255537 | ||
a0005c0005 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | ATGGC others(1690): Show |
chr12 | 108124288 | 108255537 | ||
a0006c0006 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | ATGGC others(1690): Show |
chr12 | 108124288 | 108255537 | ||
a0007c0011 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | ATGGC others(1690): Show |
chr12 | 108124288 | 108255537 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5082 | 23 | 5 | 7 | 4 | 2 | 5 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0002 | 0/0 | 5084 | 15 | 0 | 1 | 12 | 0 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0003 | 0/0 | 5082 | 14 | 5 | 3 | 6 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0004 | 1/0 | 5082 | 12 | 5 | 3 | 2 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0005 | 0/0 | 5084 | 11 | 0 | 4 | 5 | 0 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0006 | 0/0 | 5088 | 11 | 1 | 4 | 6 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5083): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0007 | 0/0 | 5082 | 10 | 1 | 1 | 5 | 3 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0008 | 0/0 | 5084 | 8 | 8 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0009 | 0/0 | 5084 | 8 | 1 | 3 | 2 | 1 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0010 | 0/0 | 5088 | 3 | 0 | 1 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5083): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0011 | 0/0 | 5082 | 7 | 7 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0012 | 0/0 | 5082 | 5 | 0 | 1 | 0 | 1 | 3 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0013 | 0/0 | 5086 | 4 | 3 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0014 | 0/0 | 5082 | 6 | 0 | 5 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0015 | 0/0 | 5092 | 5 | 2 | 1 | 0 | 1 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5087): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0016 | 0/0 | 5082 | 3 | 3 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0017 | 0/0 | 5082 | 5 | 1 | 3 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0018 | 0/0 | 5090 | 2 | 1 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5085): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0019 | 0/0 | 5082 | 3 | 2 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0020 | 0/0 | 5092 | 3 | 0 | 0 | 0 | 1 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5087): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0021 | 0/0 | 5082 | 3 | 0 | 0 | 1 | 0 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0022 | 0/0 | 5086 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0023 | 0/0 | 5086 | 3 | 2 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0024 | 0/0 | 5082 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0025 | 0/0 | 5092 | 3 | 0 | 0 | 0 | 1 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5087): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0026 | 0/0 | 5086 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0027 | 0/0 | 5084 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0028 | 0/0 | 5083 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5078): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0029 | 0/0 | 5086 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0030 | 0/0 | 5096 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5091): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0032 | 0/0 | 5084 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0033 | 0/0 | 5086 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0034 | 0/0 | 5082 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0035 | 0/0 | 5086 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0036 | 0/0 | 5086 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0038 | 0/0 | 5084 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0039 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5087): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0040 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0041 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0042 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0043 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5085): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0044 | 0/0 | 5084 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0045 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0047 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0048 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0049 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0050 | 0/0 | 5093 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5088): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0051 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0052 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0053 | 0/0 | 5122 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5117): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0054 | 0/0 | 5086 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0055 | 0/0 | 5088 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5083): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0056 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5093): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0057 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0058 | 0/0 | 5084 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0059 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0060 | 0/0 | 5086 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0061 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0062 | 0/0 | 5083 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5078): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0063 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0065 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0066 | 0/0 | 5086 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0067 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0069 | 0/0 | 5082 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0001t0070 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0003t0012 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0003t0016 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0001c0003t0022 | 0/0 | 5086 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0001c0003t0031 | 0/0 | 5084 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0001c0003t0037 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5085): Show |
chr12 | 108124288 | 108255537 |
a0001c0008t0020 | 0/0 | 5092 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5087): Show |
chr12 | 108124288 | 108255537 |
a0001c0010t0046 | 0/0 | 5082 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0002c0002t0001 | 0/0 | 5082 | 17 | 1 | 3 | 9 | 0 | 4 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0002c0002t0002 | 0/0 | 5084 | 9 | 1 | 1 | 4 | 0 | 3 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0002c0002t0003 | 0/0 | 5082 | 6 | 0 | 2 | 3 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0002c0002t0004 | 0/1 | 5082 | 2 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0002c0002t0010 | 0/0 | 5088 | 5 | 0 | 0 | 5 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5083): Show |
chr12 | 108124288 | 108255537 |
a0002c0002t0013 | 0/0 | 5086 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0002c0002t0018 | 0/0 | 5090 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5085): Show |
chr12 | 108124288 | 108255537 |
a0002c0002t0019 | 0/0 | 5082 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0002c0002t0037 | 0/0 | 5090 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5085): Show |
chr12 | 108124288 | 108255537 |
a0002c0002t0064 | 0/0 | 5086 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0002c0002t0071 | 0/0 | 5088 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5083): Show |
chr12 | 108124288 | 108255537 |
a0002c0009t0001 | 0/0 | 5082 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0003c0004t0018 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5085): Show |
chr12 | 108124288 | 108255537 |
a0003c0004t0026 | 0/0 | 5086 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0003c0004t0068 | 0/0 | 5086 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5081): Show |
chr12 | 108124288 | 108255537 |
a0004c0007t0024 | 0/0 | 5082 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0005c0005t0005 | 0/0 | 5084 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5079): Show |
chr12 | 108124288 | 108255537 |
a0006c0006t0016 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
a0007c0011t0004 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | GAGGC others(5077): Show |
chr12 | 108124288 | 108255537 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0004g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0006g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0006g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0006g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0007g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0007g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0008g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0009g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0009g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0009g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0009g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0009g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0009g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0010g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0010g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0010g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0011g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0011g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0012g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0012g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0012g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0012g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0012g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0013g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0013g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0013g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0014g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0014g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0014g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0014g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0014g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0015g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0015g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0015g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0015g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0015g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0016g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0016g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0017g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0017g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0017g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0017g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0017g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0018g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0018g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0019g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0019g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0019g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0020g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0020g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0020g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0021g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0021g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0021g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0022g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0023g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0023g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0023g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0024g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0024g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0025g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0025g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0025g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0026g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0027g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0028g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0028g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0029g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0029g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0030g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0030g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0032g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0033g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0033g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0034g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0034g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0035g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0035g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0036g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0036g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0038g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0038g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0039g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0040g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0041g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0042g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0043g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0044g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0045g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0047g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0048g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0049g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0050g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0051g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0052g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0053g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0054g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0055g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0056g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0057g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0058g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0059g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0060g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0061g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0062g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0063g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0065g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0066g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0067g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0069g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0001t0070g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0003t0012g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0003t0016g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0003t0022g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0003t0022g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0003t0031g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0003t0031g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0003t0037g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0008t0020g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0001c0010t0046g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0004g0168 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0010g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0010g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0010g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0010g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0010g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0013g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0013g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0018g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0019g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0037g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0064g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0002t0071g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0002c0009t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0003c0004t0018g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0003c0004t0026g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0003c0004t0026g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0003c0004t0068g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0004c0007t0024g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0005c0005t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0006c0006t0016g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
a0007c0011t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0163 | EUR | GBR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00099 | hp2 | a0001 | c0001 | t0058 | g0040 | EUR | GBR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00140 | hp1 | a0001 | c0001 | t0025 | g0023 | EUR | GBR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00140 | hp2 | a0001 | c0001 | t0012 | g0032 | EUR | GBR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00280 | hp1 | a0001 | c0001 | t0007 | g0029 | EUR | FIN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00280 | hp2 | a0002 | c0002 | t0003 | g0242 | EUR | FIN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00323 | hp1 | a0001 | c0001 | t0007 | g0019 | EUR | FIN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00323 | hp2 | a0001 | c0001 | t0017 | g0094 | EUR | FIN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00438 | hp1 | a0004 | c0007 | t0024 | g0028 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00438 | hp2 | a0001 | c0001 | t0010 | g0189 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00558 | hp1 | a0002 | c0002 | t0003 | g0180 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00558 | hp2 | a0002 | c0002 | t0010 | g0129 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00609 | hp2 | a0001 | c0001 | t0021 | g0264 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00639 | hp1 | a0001 | c0001 | t0013 | g0204 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0102 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00642 | hp1 | a0001 | c0001 | t0009 | g0021 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0090 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00733 | hp2 | a0005 | c0005 | t0005 | g0166 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00735 | hp1 | a0002 | c0002 | t0019 | g0083 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0160 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0203 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG00738 | hp2 | a0001 | c0001 | t0050 | g0119 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01069 | hp1 | a0002 | c0002 | t0018 | g0042 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01074 | hp1 | a0002 | c0002 | t0003 | g0191 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01081 | hp2 | a0002 | c0002 | t0064 | g0205 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01099 | hp1 | a0001 | c0001 | t0015 | g0228 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0261 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01109 | hp1 | a0001 | c0001 | t0060 | g0267 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0165 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01167 | hp1 | a0001 | c0001 | t0017 | g0213 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01167 | hp2 | a0001 | c0001 | t0029 | g0226 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01168 | hp2 | a0001 | c0008 | t0020 | g0220 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01169 | hp1 | a0001 | c0001 | t0029 | g0227 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01175 | hp2 | a0002 | c0002 | t0003 | g0240 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0034 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01243 | hp2 | a0001 | c0003 | t0031 | g0055 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0158 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01256 | hp2 | a0001 | c0001 | t0009 | g0003 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01257 | hp1 | a0001 | c0001 | t0032 | g0004 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0116 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01258 | hp2 | a0001 | c0001 | t0009 | g0003 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01261 | hp2 | a0002 | c0002 | t0071 | g0097 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0164 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01346 | hp2 | a0001 | c0001 | t0014 | g0009 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01358 | hp1 | a0001 | c0001 | t0032 | g0004 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01361 | hp1 | a0001 | c0001 | t0006 | g0117 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01361 | hp2 | a0001 | c0001 | t0017 | g0095 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01433 | hp1 | a0001 | c0001 | t0014 | g0009 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01433 | hp2 | a0001 | c0001 | t0017 | g0096 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01515 | hp1 | a0001 | c0001 | t0020 | g0085 | EUR | IBS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01516 | hp1 | a0001 | c0001 | t0015 | g0091 | EUR | IBS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01516 | hp2 | a0001 | c0001 | t0009 | g0022 | EUR | IBS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0113 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01891 | hp1 | a0001 | c0001 | t0041 | g0156 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01943 | hp1 | a0001 | c0001 | t0012 | g0044 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01943 | hp2 | a0001 | c0001 | t0034 | g0250 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01952 | hp1 | a0001 | c0001 | t0014 | g0010 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01952 | hp2 | a0001 | c0001 | t0006 | g0161 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0120 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01981 | hp1 | a0001 | c0001 | t0028 | g0231 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0114 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01993 | hp1 | a0001 | c0001 | t0014 | g0132 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG01993 | hp2 | a0001 | c0001 | t0028 | g0167 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02015 | hp2 | a0002 | c0002 | t0013 | g0187 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02055 | hp2 | a0001 | c0001 | t0015 | g0151 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02080 | hp1 | a0002 | c0002 | t0010 | g0214 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02135 | hp2 | a0001 | c0001 | t0069 | g0136 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0199 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0154 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02148 | hp1 | a0001 | c0001 | t0023 | g0232 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02148 | hp2 | a0002 | c0002 | t0037 | g0078 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02165 | hp1 | a0002 | c0002 | t0013 | g0188 | EAS | CDX | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | CDX | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02257 | hp2 | a0001 | c0001 | t0016 | g0048 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02258 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02258 | hp2 | a0001 | c0001 | t0040 | g0012 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02273 | hp1 | a0001 | c0001 | t0014 | g0139 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02280 | hp1 | a0001 | c0001 | t0022 | g0087 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02280 | hp2 | a0001 | c0001 | t0008 | g0253 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02451 | hp1 | a0001 | c0003 | t0031 | g0054 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02451 | hp2 | a0001 | c0001 | t0065 | g0241 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02572 | hp1 | a0001 | c0001 | t0011 | g0125 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02572 | hp2 | a0001 | c0001 | t0035 | g0070 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02615 | hp1 | a0001 | c0003 | t0022 | g0236 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02615 | hp2 | a0001 | c0001 | t0008 | g0086 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02622 | hp1 | a0001 | c0001 | t0030 | g0157 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02622 | hp2 | a0001 | c0001 | t0036 | g0064 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02630 | hp1 | a0001 | c0001 | t0049 | g0128 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0092 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02647 | hp1 | a0001 | c0001 | t0019 | g0061 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02647 | hp2 | a0001 | c0003 | t0037 | g0065 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02683 | hp1 | a0001 | c0001 | t0012 | g0045 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0093 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02717 | hp1 | a0001 | c0001 | t0042 | g0223 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0260 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0053 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02735 | hp1 | a0001 | c0001 | t0021 | g0159 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0207 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02738 | hp1 | a0001 | c0001 | t0062 | g0074 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02738 | hp2 | a0001 | c0001 | t0021 | g0256 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0088 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02809 | hp2 | a0001 | c0003 | t0012 | g0049 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02818 | hp1 | a0001 | c0001 | t0039 | g0152 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02818 | hp2 | a0001 | c0001 | t0018 | g0031 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02886 | hp1 | a0001 | c0001 | t0019 | g0062 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02886 | hp2 | a0001 | c0001 | t0034 | g0224 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02895 | hp1 | a0001 | c0001 | t0033 | g0037 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02895 | hp2 | a0001 | c0001 | t0027 | g0013 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02897 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02897 | hp2 | a0001 | c0001 | t0027 | g0013 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02922 | hp1 | a0001 | c0001 | t0011 | g0060 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0052 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02965 | hp1 | a0001 | c0001 | t0011 | g0122 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02965 | hp2 | a0001 | c0001 | t0036 | g0101 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02970 | hp1 | a0001 | c0001 | t0059 | g0268 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02970 | hp2 | a0001 | c0001 | t0017 | g0212 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02976 | hp1 | a0001 | c0001 | t0013 | g0247 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02976 | hp2 | a0001 | c0001 | t0067 | g0063 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03017 | hp1 | a0001 | c0001 | t0012 | g0033 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03017 | hp2 | a0001 | c0001 | t0020 | g0135 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0126 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03041 | hp2 | a0001 | c0001 | t0013 | g0246 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03098 | hp1 | a0003 | c0004 | t0018 | g0056 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03098 | hp2 | a0001 | c0001 | t0016 | g0269 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03130 | hp1 | a0001 | c0001 | t0056 | g0265 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03130 | hp2 | a0001 | c0001 | t0011 | g0124 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0229 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03195 | hp1 | a0001 | c0001 | t0048 | g0153 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03195 | hp2 | a0001 | c0001 | t0047 | g0100 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03209 | hp1 | a0001 | c0001 | t0033 | g0038 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03209 | hp2 | a0001 | c0001 | t0030 | g0127 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03225 | hp2 | a0003 | c0004 | t0026 | g0058 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0145 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03239 | hp2 | a0001 | c0001 | t0012 | g0036 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03453 | hp1 | a0001 | c0001 | t0035 | g0252 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03453 | hp2 | a0003 | c0004 | t0068 | g0217 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03486 | hp1 | a0001 | c0003 | t0022 | g0257 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03486 | hp2 | a0001 | c0001 | t0051 | g0123 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03490 | hp1 | a0001 | c0001 | t0018 | g0018 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03490 | hp2 | a0001 | c0001 | t0025 | g0046 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03492 | hp1 | a0001 | c0001 | t0025 | g0035 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0211 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03516 | hp1 | a0001 | c0001 | t0054 | g0051 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03540 | hp1 | a0001 | c0001 | t0023 | g0146 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03540 | hp2 | a0001 | c0001 | t0013 | g0248 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03579 | hp1 | a0001 | c0001 | t0023 | g0150 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03579 | hp2 | a0001 | c0001 | t0026 | g0039 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03688 | hp2 | a0001 | c0001 | t0044 | g0254 | SAS | STU | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03704 | hp1 | a0001 | c0001 | t0020 | g0080 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0210 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03710 | hp1 | a0001 | c0001 | t0019 | g0208 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0215 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0255 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03927 | hp2 | a0001 | c0001 | t0009 | g0043 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03942 | hp1 | a0001 | c0001 | t0053 | g0024 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0183 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0142 | SAS | STU | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG04204 | hp2 | a0001 | c0001 | t0015 | g0169 | SAS | STU | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | YRI | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18522 | hp2 | a0001 | c0001 | t0063 | g0069 | AFR | YRI | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | CHB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18612 | hp2 | a0001 | c0001 | t0007 | g0026 | EAS | CHB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18906 | hp1 | a0001 | c0001 | t0061 | g0266 | AFR | YRI | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | YRI | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18940 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18941 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18941 | hp2 | a0001 | c0001 | t0024 | g0025 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18944 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18948 | hp1 | a0002 | c0002 | t0003 | g0259 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18948 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18949 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18951 | hp1 | a0001 | c0001 | t0055 | g0027 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18952 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18953 | hp1 | a0001 | c0001 | t0052 | g0235 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18953 | hp2 | a0002 | c0002 | t0010 | g0237 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18960 | hp2 | a0001 | c0001 | t0007 | g0017 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18971 | hp2 | a0002 | c0002 | t0010 | g0195 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18978 | hp1 | a0002 | c0009 | t0001 | g0178 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18981 | hp1 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18982 | hp1 | a0002 | c0002 | t0004 | g0073 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18982 | hp2 | a0001 | c0001 | t0038 | g0184 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18994 | hp1 | a0001 | c0001 | t0038 | g0185 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18994 | hp2 | a0001 | c0001 | t0045 | g0172 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18998 | hp1 | a0001 | c0001 | t0024 | g0030 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA18998 | hp2 | a0001 | c0001 | t0070 | g0010 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19000 | hp1 | a0001 | c0001 | t0009 | g0041 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19009 | hp2 | a0001 | c0001 | t0014 | g0148 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19012 | hp1 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | LWK | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19043 | hp2 | a0001 | c0001 | t0043 | g0147 | AFR | LWK | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19068 | hp1 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19068 | hp2 | a0002 | c0002 | t0010 | g0182 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19079 | hp2 | a0001 | c0001 | t0006 | g0233 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19081 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19087 | hp1 | a0001 | c0001 | t0010 | g0131 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19088 | hp1 | a0001 | c0010 | t0046 | g0230 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA19088 | hp2 | a0002 | c0002 | t0003 | g0198 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA20129 | hp1 | a0006 | c0006 | t0016 | g0050 | AFR | ASW | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA20129 | hp2 | a0007 | c0011 | t0004 | g0099 | AFR | ASW | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA20752 | hp1 | a0001 | c0001 | t0007 | g0020 | EUR | TSI | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02109 | hp1 | a0001 | c0001 | t0057 | g0251 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02109 | hp2 | a0003 | c0004 | t0026 | g0057 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02486 | hp1 | a0001 | c0003 | t0016 | g0059 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0111 | AFR | USA | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
HG06807 | hp2 | a0001 | c0001 | t0015 | g0089 | AFR | USA | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA21309 | hp1 | a0001 | c0001 | t0016 | g0047 | AFR | LWK | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
NA21309 | hp2 | a0001 | c0001 | t0066 | g0108 | AFR | LWK | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
homoSapiens | chm13v2 | a0002 | c0002 | t0004 | g0168 | REF | REF | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0162 | REF | REF | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:108195981 | C | T | 1 | a0007 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.149C>T | p.Ala50Val | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 1339/5082 | 149/1698 | 50/565 | chr12 | 108195981 | |||
chr12:108196134 | G | A | 1 | a0005 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.302G>A | p.Arg101Lys | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 1492/5082 | 302/1698 | 101/565 | chr12 | 108196134 | |||
chr12:108196188 | T | C | 1 | a0003 | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.356T>C | p.Val119Ala | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 1546/5082 | 356/1698 | 119/565 | chr12 | 108196188 | |||
chr12:108224769 | G | A | 1 | a0006 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.713G>A | p.Arg238His | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/9 | 1903/5082 | 713/1698 | 238/565 | chr12 | 108224769 | |||
chr12:108224853 | C | T | 1 | a0002 | 46 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(43): Show |
missense_variant | MODERATE | c.797C>T | p.Thr266Ile | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/9 | 1987/5082 | 797/1698 | 266/565 | chr12 | 108224853 | |||
chr12:108227106 | G | C | 1 | a0004 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.921G>C | p.Glu307Asp | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/9 | 2111/5082 | 921/1698 | 307/565 | chr12 | 108227106 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:108195985 | C | T | 1 | a0001c0010 | 1 | NA19088.hp1 | synonymous_variant | LOW | c.153C>T | p.Asn51Asn | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 1343/5082 | 153/1698 | 51/565 | chr12 | 108195985 | |||
chr12:108210151 | C | T | 1 | a0002c0009 | 1 | NA18978.hp1 | synonymous_variant | LOW | c.528C>T | p.Gly176Gly | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/9 | 1718/5082 | 528/1698 | 176/565 | chr12 | 108210151 | |||
chr12:108224776 | C | G | 1 | a0001c0008 | 1 | HG01168.hp2 | synonymous_variant | LOW | c.720C>G | p.Pro240Pro | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/9 | 1910/5082 | 720/1698 | 240/565 | chr12 | 108224776 | |||
chr12:108224839 | C | T | 1 | a0001c0003 | 7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
synonymous_variant | LOW | c.783C>T | p.Cys261Cys | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/9 | 1973/5082 | 783/1698 | 261/565 | chr12 | 108224839 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:108129413 | C | T | 2 | a0001c0001t0017 a0002c0002t0071 |
6 | HG00323.hp2 HG01167.hp1 HG01261.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1065C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | chr12 | 108129413 | |||||||
chr12:108129421 | C | T | 34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(31): Show |
137 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1057C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | chr12 | 108129421 | |||||||
chr12:108129437 | C | T | 1 | a0001c0001t0058 | 1 | HG00099.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1041C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | chr12 | 108129437 | |||||||
chr12:108129442 | C | A | 1 | a0001c0001t0058 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1036C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | 66391 | chr12 | 108129442 | ||||||
chr12:108129444 | C | T | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(28): Show |
134 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1034C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | chr12 | 108129444 | |||||||
chr12:108129471 | A | G | 3 | a0001c0001t0034 a0001c0001t0035 a0001c0001t0057 |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-1007A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | 66362 | chr12 | 108129471 | ||||||
chr12:108129559 | C | G | 3 | a0001c0001t0059 a0001c0001t0060 a0001c0001t0061 |
3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-919C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | 66274 | chr12 | 108129559 | ||||||
chr12:108129744 | G | T | 2 | a0001c0001t0014 a0001c0001t0070 |
7 | HG01346.hp2 HG01433.hp1 HG01952.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-734G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | chr12 | 108129744 | |||||||
chr12:108129891 | A | C | 26 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0012 others(23): Show |
56 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(53): Show |
5_prime_UTR_variant | MODIFIER | c.-587A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | 65942 | chr12 | 108129891 | ||||||
chr12:108195393 | G | A | 1 | a0001c0001t0027 | 2 | HG02895.hp2 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-440G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 440 | chr12 | 108195393 | ||||||
chr12:108195637 | A | G | 1 | a0001c0001t0069 | 1 | HG02135.hp2 | 5_prime_UTR_variant | MODIFIER | c.-196A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 196 | chr12 | 108195637 | ||||||
chr12:108195763 | C | G | 1 | a0001c0001t0061 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 70 | chr12 | 108195763 | ||||||
chr12:108248357 | G | T | 2 | a0001c0001t0038 a0001c0001t0052 |
3 | NA18953.hp1 NA18982.hp2 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*14G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 14 | chr12 | 108248357 | ||||||
chr12:108248385 | C | T | 1 | a0001c0001t0069 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 42 | chr12 | 108248385 | ||||||
chr12:108248623 | C | T | 35 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0011 others(32): Show |
79 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*280C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 280 | chr12 | 108248623 | ||||||
chr12:108248821 | C | T | 1 | a0001c0001t0066 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 478 | chr12 | 108248821 | ||||||
chr12:108248988 | C | A | 1 | a0001c0001t0047 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*645C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 645 | chr12 | 108248988 | ||||||
chr12:108249043 | A | G | 1 | a0001c0001t0065 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*700A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 700 | chr12 | 108249043 | ||||||
chr12:108249113 | C | A | 11 | a0001c0001t0008 a0001c0001t0027 a0001c0001t0028 others(8): Show |
22 | HG00099.hp2 HG01243.hp2 HG01257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*770C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 770 | chr12 | 108249113 | ||||||
chr12:108249114 | C | A | 11 | a0001c0001t0008 a0001c0001t0027 a0001c0001t0028 others(8): Show |
22 | HG00099.hp2 HG01243.hp2 HG01257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*771C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 771 | chr12 | 108249114 | ||||||
chr12:108249115 | TCA | T | 11 | a0001c0001t0008 a0001c0001t0027 a0001c0001t0028 others(8): Show |
22 | HG00099.hp2 HG01243.hp2 HG01257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*773_*774delCA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 773 | chr12 | 108249115 | ||||||
chr12:108249280 | G | A | 30 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0011 others(27): Show |
72 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*937G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 937 | chr12 | 108249280 | ||||||
chr12:108249295 | G | T | 11 | a0001c0001t0008 a0001c0001t0027 a0001c0001t0028 others(8): Show |
22 | HG00099.hp2 HG01257.hp1 HG01358.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*952G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 952 | chr12 | 108249295 | ||||||
chr12:108249339 | A | G | 1 | a0001c0001t0040 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*996A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 996 | chr12 | 108249339 | ||||||
chr12:108249400 | T | C | 2 | a0001c0001t0041 a0001c0001t0057 |
2 | HG01891.hp1 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1057T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1057 | chr12 | 108249400 | ||||||
chr12:108249641 | A | C | 3 | a0001c0001t0024 a0001c0010t0046 a0004c0007t0024 |
4 | HG00438.hp1 NA18941.hp2 NA18998.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1298A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1298 | chr12 | 108249641 | ||||||
chr12:108249689 | G | T | 1 | a0001c0001t0045 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1346 | chr12 | 108249689 | ||||||
chr12:108249776 | C | T | 25 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0013 others(22): Show |
59 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1433C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1433 | chr12 | 108249776 | ||||||
chr12:108249779 | C | G | 1 | a0001c0001t0044 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1436C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1436 | chr12 | 108249779 | ||||||
chr12:108249927 | AT | A | 2 | a0001c0001t0028 a0001c0001t0062 |
3 | HG01981.hp1 HG01993.hp2 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1589delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1589 | INFO_REALIGN_3_PRIME | chr12 | 108249927 | |||||
chr12:108249999 | A | AGAAGGAA others(33): Show |
1 | a0001c0001t0053 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1658_*1659insAGGA others(36): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1659 | INFO_REALIGN_3_PRIME | chr12 | 108249999 | |||||
chr12:108250171 | A | AGT | 13 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(10): Show |
53 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1855_*1856dupGT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | |||||
chr12:108250171 | A | AGTGT | 26 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0022 others(23): Show |
49 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1853_*1856dupGTGT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | |||||
chr12:108250171 | A | AGTGTGT | 5 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0055 others(2): Show |
21 | HG00438.hp2 HG00558.hp2 HG00639.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1851_*1856dupGTGT others(2): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | |||||
chr12:108250171 | A | AGTGTGTG others(1): Show |
6 | a0001c0001t0018 a0001c0001t0043 a0001c0003t0037 others(3): Show |
7 | HG01069.hp1 HG02148.hp2 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1849_*1856dupGTGT others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | |||||
chr12:108250171 | A | AGTGTGTG others(3): Show |
4 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0025 others(1): Show |
12 | HG00140.hp1 HG01099.hp1 HG01168.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1847_*1856dupGTGT others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | |||||
chr12:108250171 | A | AGTGTGTG others(5): Show |
1 | a0001c0001t0039 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1845_*1856dupGTGT others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | |||||
chr12:108250171 | A | AGTGTGTG others(7): Show |
1 | a0001c0001t0030 | 2 | HG02622.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1843_*1856dupGTGT others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | |||||
chr12:108250171 | A | AGTGTGTG others(9): Show |
1 | a0001c0001t0056 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1841_*1856dupGTGT others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | |||||
chr12:108250198 | G | A | 1 | a0001c0001t0042 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1855G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1855 | chr12 | 108250198 | ||||||
chr12:108250199 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0050 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1856_*1857insGTGT others(7): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | chr12 | 108250199 | ||||||
chr12:108250200 | A | G | 19 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0011 others(16): Show |
64 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1857A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | chr12 | 108250200 | ||||||
chr12:108250201 | T | A | 1 | a0001c0001t0042 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1858T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1858 | chr12 | 108250201 | ||||||
chr12:108250202 | G | A | 7 | a0001c0001t0011 a0001c0001t0016 a0001c0001t0019 others(4): Show |
16 | HG00735.hp1 HG02257.hp2 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1859G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1859 | chr12 | 108250202 | ||||||
chr12:108250202 | G | C | 2 | a0001c0001t0008 a0001c0001t0063 |
2 | HG06807.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1859G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1859 | chr12 | 108250202 | ||||||
chr12:108250202 | G | GTA | 12 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0016 others(9): Show |
41 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1859_*1860insTA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1860 | chr12 | 108250202 | ||||||
chr12:108250202 | G | GTGTA | 2 | a0001c0001t0003 a0001c0001t0017 |
3 | HG01167.hp1 HG01261.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1859_*1860insTGTA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1860 | chr12 | 108250202 | ||||||
chr12:108250202 | G | GTGTGTA | 2 | a0001c0001t0003 a0001c0001t0007 |
3 | HG02717.hp2 HG02723.hp1 NA18960.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1859_*1860insTGTG others(2): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1860 | chr12 | 108250202 | ||||||
chr12:108250203 | A | T | 18 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0011 others(15): Show |
63 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1860A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1860 | chr12 | 108250203 | ||||||
chr12:108250381 | T | A | 1 | a0001c0001t0042 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2038T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 2038 | chr12 | 108250381 | ||||||
chr12:108250412 | T | C | 67 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(64): Show |
160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*2069T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 2069 | chr12 | 108250412 | ||||||
chr12:108250476 | T | C | 9 | a0001c0001t0011 a0001c0001t0016 a0001c0001t0019 others(6): Show |
19 | HG00735.hp1 HG02257.hp2 HG02486.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2133T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 2133 | chr12 | 108250476 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:108129976 | G | A | 37 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(34): Show |
40 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.-552+50G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108129976 | |||||||
chr12:108130261 | G | T | 43 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(40): Show |
46 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.-552+335G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130261 | |||||||
chr12:108130329 | T | A | 54 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(51): Show |
57 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.-552+403T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130329 | |||||||
chr12:108130342 | G | A | 5 | a0001c0001t0007g0053 a0001c0001t0009g0052 a0001c0001t0054g0051 others(2): Show |
5 | HG02723.hp1 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+416G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130342 | |||||||
chr12:108130475 | G | GGT | 33 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0001t0001g0249 others(30): Show |
35 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.-552+594_-552+595d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | ||||||
chr12:108130475 | G | GGTGT | 11 | a0001c0001t0003g0258 a0001c0001t0003g0260 a0001c0001t0005g0255 others(8): Show |
11 | HG02257.hp2 HG02280.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-552+592_-552+595d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | ||||||
chr12:108130475 | G | GTGT | 3 | a0001c0001t0003g0263 a0002c0002t0002g0261 a0002c0002t0002g0262 |
3 | HG01099.hp2 HG01261.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-552+549_-552+550i others(5): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130475 | |||||||
chr12:108130475 | GGT | G | 51 | a0001c0001t0001g0107 a0001c0001t0001g0133 a0001c0001t0001g0143 others(48): Show |
53 | HG00423.hp1 HG00558.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.-552+594_-552+595d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | ||||||
chr12:108130475 | GGTGT | G | 15 | a0001c0001t0001g0098 a0001c0001t0002g0008 a0001c0001t0002g0104 others(12): Show |
16 | HG00639.hp2 HG01069.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.-552+592_-552+595d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | ||||||
chr12:108130475 | GGTGTGT | G | 30 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0006g0088 others(27): Show |
32 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.-552+590_-552+595d others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | ||||||
chr12:108130475 | GGTGTGTG others(1): Show |
G | 27 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(24): Show |
28 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.-552+588_-552+595d others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | ||||||
chr12:108130475 | GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0002g0071 a0001c0001t0056g0265 |
2 | HG01069.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+586_-552+595d others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | ||||||
chr12:108130475 | GGTGTGTG others(5): Show |
G | 12 | a0001c0001t0001g0005 a0001c0001t0003g0006 a0001c0001t0003g0066 others(9): Show |
14 | HG01081.hp1 HG01175.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-552+584_-552+595d others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | ||||||
chr12:108130475 | GGTGTGTG others(15): Show |
G | 4 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(1): Show |
5 | NA18944.hp1 NA18952.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+574_-552+595d others(24): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | ||||||
chr12:108130479 | T | G | 1 | a0001c0001t0011g0060 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-552+553T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130479 | |||||||
chr12:108130481 | T | G | 1 | a0001c0001t0024g0030 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-552+555T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130481 | |||||||
chr12:108130483 | T | G | 6 | a0001c0001t0007g0026 a0001c0001t0007g0029 a0001c0001t0021g0264 others(3): Show |
6 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.-552+557T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130483 | |||||||
chr12:108130485 | T | G | 7 | a0001c0001t0007g0019 a0001c0001t0007g0020 a0001c0001t0009g0021 others(4): Show |
7 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.-552+559T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130485 | |||||||
chr12:108130499 | T | G | 4 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(1): Show |
5 | NA18944.hp1 NA18952.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+573T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130499 | |||||||
chr12:108130765 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-552+839G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130765 | |||||||
chr12:108130834 | A | G | 51 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(48): Show |
54 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.-552+908A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130834 | |||||||
chr12:108130931 | A | G | 51 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(48): Show |
54 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.-552+1005A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130931 | |||||||
chr12:108130957 | A | G | 51 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(48): Show |
54 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.-552+1031A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130957 | |||||||
chr12:108130962 | C | T | 2 | a0001c0001t0032g0004 a0001c0001t0058g0040 |
3 | HG00099.hp2 HG01257.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-552+1036C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130962 | |||||||
chr12:108131072 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-552+1146T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131072 | |||||||
chr12:108131095 | C | T | 56 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(53): Show |
59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.-552+1169C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131095 | |||||||
chr12:108131133 | G | A | 56 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(53): Show |
59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.-552+1207G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131133 | |||||||
chr12:108131648 | G | A | 1 | a0001c0001t0066g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-552+1722G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131648 | |||||||
chr12:108131649 | A | G | 1 | a0001c0001t0066g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-552+1723A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131649 | |||||||
chr12:108131668 | A | G | 57 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(54): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+1742A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131668 | |||||||
chr12:108131738 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-552+1812G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131738 | |||||||
chr12:108131756 | C | T | 57 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(54): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+1830C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131756 | |||||||
chr12:108131818 | C | G | 57 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(54): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+1892C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131818 | |||||||
chr12:108131823 | A | C | 1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+1897A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131823 | |||||||
chr12:108131898 | A | G | 1 | a0001c0001t0014g0148 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-552+1972A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131898 | |||||||
chr12:108131950 | C | T | 8 | a0001c0001t0007g0053 a0001c0001t0009g0052 a0001c0001t0054g0051 others(5): Show |
8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-552+2024C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131950 | |||||||
chr12:108132036 | T | TTG | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+2124_-552+212 others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108132036 | ||||||
chr12:108132041 | TG | T | 3 | a0001c0001t0023g0146 a0001c0001t0042g0223 a0001c0001t0043g0147 |
3 | HG02717.hp1 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-552+2116delG | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132041 | |||||||
chr12:108132135 | A | AT | 130 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(127): Show |
134 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-552+2216dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108132135 | ||||||
chr12:108132147 | G | A | 8 | a0001c0001t0007g0053 a0001c0001t0009g0052 a0001c0001t0054g0051 others(5): Show |
8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-552+2221G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132147 | |||||||
chr12:108132296 | A | G | 211 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(208): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.-552+2370A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132296 | |||||||
chr12:108132529 | C | T | 132 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(129): Show |
136 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-552+2603C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132529 | |||||||
chr12:108132559 | T | C | 235 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(232): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.-552+2633T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132559 | |||||||
chr12:108132608 | C | T | 58 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(55): Show |
61 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.-552+2682C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132608 | |||||||
chr12:108132629 | CAT | C | 4 | a0001c0001t0059g0268 a0001c0001t0060g0267 a0001c0001t0061g0266 others(1): Show |
4 | HG01109.hp1 HG02970.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-552+2704_-552+270 others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132629 | |||||||
chr12:108132669 | C | G | 57 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(54): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+2743C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132669 | |||||||
chr12:108132694 | T | C | 2 | a0001c0001t0016g0269 a0001c0001t0056g0265 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+2768T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132694 | |||||||
chr12:108132721 | A | G | 57 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(54): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+2795A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132721 | |||||||
chr12:108132759 | G | A | 57 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(54): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+2833G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132759 | |||||||
chr12:108132778 | G | A | 7 | a0001c0001t0011g0014 a0001c0001t0011g0122 a0001c0001t0011g0124 others(4): Show |
8 | HG02280.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-552+2852G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132778 | |||||||
chr12:108132827 | A | G | 5 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0011g0092 others(2): Show |
5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+2901A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132827 | |||||||
chr12:108132914 | A | G | 3 | a0001c0001t0059g0268 a0001c0001t0060g0267 a0001c0001t0061g0266 |
3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+2988A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132914 | |||||||
chr12:108133018 | C | T | 1 | a0001c0001t0054g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-552+3092C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133018 | |||||||
chr12:108133073 | G | A | 57 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(54): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+3147G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133073 | |||||||
chr12:108133180 | G | A | 1 | a0001c0001t0004g0225 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-552+3254G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133180 | |||||||
chr12:108133240 | G | A | 1 | a0001c0001t0011g0122 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-552+3314G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133240 | |||||||
chr12:108133294 | G | A | 1 | a0001c0001t0004g0114 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-552+3368G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133294 | |||||||
chr12:108133319 | C | T | 1 | a0001c0001t0043g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-552+3393C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133319 | |||||||
chr12:108133320 | G | A | 57 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(54): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+3394G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133320 | |||||||
chr12:108133374 | C | T | 4 | a0001c0001t0017g0094 a0001c0001t0017g0095 a0001c0001t0017g0096 others(1): Show |
4 | HG00323.hp2 HG01261.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+3448C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133374 | |||||||
chr12:108133411 | G | T | 4 | a0001c0001t0002g0008 a0001c0001t0002g0104 a0001c0001t0002g0105 others(1): Show |
5 | HG02015.hp1 HG02165.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.-552+3485G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133411 | |||||||
chr12:108133539 | C | T | 2 | a0001c0001t0016g0269 a0001c0001t0056g0265 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+3613C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133539 | |||||||
chr12:108133540 | C | T | 1 | a0002c0002t0004g0073 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-552+3614C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133540 | |||||||
chr12:108133623 | C | T | 1 | a0001c0001t0004g0121 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-552+3697C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133623 | |||||||
chr12:108133686 | C | T | 39 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(36): Show |
42 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.-552+3760C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133686 | |||||||
chr12:108133716 | G | A | 3 | a0001c0001t0059g0268 a0001c0001t0060g0267 a0001c0001t0061g0266 |
3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+3790G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133716 | |||||||
chr12:108133784 | G | A | 187 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(184): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.-552+3858G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133784 | |||||||
chr12:108133807 | G | A | 1 | a0003c0004t0018g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-552+3881G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133807 | |||||||
chr12:108134392 | C | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-552+4466C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134392 | |||||||
chr12:108134413 | C | T | 1 | a0001c0001t0023g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-552+4487C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134413 | |||||||
chr12:108134470 | A | G | 2 | a0001c0001t0016g0269 a0001c0001t0056g0265 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+4544A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134470 | |||||||
chr12:108134494 | T | G | 1 | a0001c0001t0012g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-552+4568T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134494 | |||||||
chr12:108134512 | C | T | 1 | a0002c0002t0002g0222 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-552+4586C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134512 | |||||||
chr12:108134618 | A | G | 1 | a0001c0001t0004g0225 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-552+4692A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134618 | |||||||
chr12:108134734 | G | A | 2 | a0001c0001t0008g0012 a0001c0001t0040g0012 |
2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-552+4808G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134734 | |||||||
chr12:108134809 | A | T | 2 | a0001c0001t0016g0269 a0001c0001t0056g0265 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+4883A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134809 | |||||||
chr12:108134937 | G | A | 1 | a0001c0001t0023g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-552+5011G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134937 | |||||||
chr12:108135055 | G | A | 1 | a0001c0001t0004g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-552+5129G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135055 | |||||||
chr12:108135083 | A | G | 3 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 |
3 | HG02109.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-552+5157A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135083 | |||||||
chr12:108135126 | TTCCA | T | 11 | a0001c0001t0007g0053 a0001c0001t0009g0052 a0001c0001t0054g0051 others(8): Show |
11 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-552+5204_-552+520 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108135126 | ||||||
chr12:108135166 | A | ATCCATCC others(1): Show |
11 | a0001c0001t0001g0005 a0001c0001t0003g0006 a0001c0001t0003g0066 others(8): Show |
13 | HG01081.hp1 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-552+5243_-552+524 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108135166 | ||||||
chr12:108135308 | A | G | 39 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(36): Show |
42 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.-552+5382A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135308 | |||||||
chr12:108135313 | A | G | 7 | a0001c0001t0011g0014 a0001c0001t0011g0122 a0001c0001t0011g0124 others(4): Show |
8 | HG02280.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-552+5387A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135313 | |||||||
chr12:108135471 | C | T | 2 | a0001c0001t0042g0223 a0001c0001t0043g0147 |
2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-552+5545C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135471 | |||||||
chr12:108135481 | T | A | 1 | a0001c0001t0018g0031 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-552+5555T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135481 | |||||||
chr12:108135565 | C | T | 3 | a0001c0001t0059g0268 a0001c0001t0060g0267 a0001c0001t0061g0266 |
3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+5639C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135565 | |||||||
chr12:108135594 | G | A | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+5668G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135594 | |||||||
chr12:108135789 | C | T | 1 | a0002c0002t0002g0142 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-552+5863C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135789 | |||||||
chr12:108135808 | C | T | 1 | a0001c0001t0030g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-552+5882C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135808 | |||||||
chr12:108135864 | G | GA | 198 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(195): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.-552+5938_-552+593 others(5): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135864 | |||||||
chr12:108135865 | G | C | 198 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(195): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.-552+5939G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135865 | |||||||
chr12:108135988 | C | T | 2 | a0001c0001t0016g0269 a0001c0001t0056g0265 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+6062C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135988 | |||||||
chr12:108136012 | G | A | 1 | a0001c0001t0066g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-552+6086G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136012 | |||||||
chr12:108136064 | G | A | 1 | a0002c0002t0002g0261 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-552+6138G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136064 | |||||||
chr12:108136306 | C | T | 3 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 |
3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-552+6380C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136306 | |||||||
chr12:108136318 | T | G | 1 | a0001c0001t0002g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-552+6392T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136318 | |||||||
chr12:108136334 | G | GTCCCTTC others(19): Show |
1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+6412_-552+641 others(30): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108136334 | ||||||
chr12:108136334 | G | GTCCCTTC others(19): Show |
192 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(189): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.-552+6412_-552+641 others(30): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108136334 | ||||||
chr12:108136371 | C | G | 1 | a0001c0001t0066g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-552+6445C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136371 | |||||||
chr12:108136510 | G | A | 1 | a0002c0002t0001g0175 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-552+6584G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136510 | |||||||
chr12:108136722 | CCCGTGTT others(46): Show |
C | 3 | a0001c0001t0026g0039 a0001c0001t0033g0037 a0001c0001t0033g0038 |
3 | HG02895.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-552+6797_-552+684 others(57): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136722 | |||||||
chr12:108136745 | C | T | 5 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0011g0092 others(2): Show |
5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+6819C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136745 | |||||||
chr12:108136746 | G | C | 56 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(53): Show |
59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.-552+6820G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136746 | |||||||
chr12:108136760 | C | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-552+6834C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136760 | |||||||
chr12:108136760 | C | T | 1 | a0001c0001t0007g0053 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-552+6834C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136760 | |||||||
chr12:108136804 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-552+6878C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136804 | |||||||
chr12:108136904 | G | T | 11 | a0001c0001t0007g0053 a0001c0001t0009g0052 a0001c0001t0054g0051 others(8): Show |
11 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-552+6978G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136904 | |||||||
chr12:108137076 | C | G | 9 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0006g0088 others(6): Show |
9 | HG00642.hp2 HG01516.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-552+7150C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137076 | |||||||
chr12:108137086 | C | T | 1 | a0001c0001t0053g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-552+7160C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137086 | |||||||
chr12:108137214 | A | C | 1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+7288A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137214 | |||||||
chr12:108137245 | T | C | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+7319T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137245 | |||||||
chr12:108137270 | T | C | 44 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(41): Show |
47 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.-552+7344T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137270 | |||||||
chr12:108137336 | C | T | 3 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 |
3 | HG02109.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-552+7410C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137336 | |||||||
chr12:108137640 | G | A | 3 | a0001c0001t0059g0268 a0001c0001t0060g0267 a0001c0001t0061g0266 |
3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+7714G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137640 | |||||||
chr12:108137700 | G | A | 1 | a0002c0002t0010g0129 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-552+7774G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137700 | |||||||
chr12:108137742 | T | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-552+7816T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137742 | |||||||
chr12:108137824 | G | T | 59 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(56): Show |
62 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.-552+7898G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137824 | |||||||
chr12:108137883 | C | T | 1 | a0001c0001t0066g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-552+7957C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137883 | |||||||
chr12:108138273 | A | G | 15 | a0001c0001t0007g0053 a0001c0001t0009g0052 a0001c0001t0016g0269 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-552+8347A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138273 | |||||||
chr12:108138376 | G | A | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+8450G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138376 | |||||||
chr12:108138494 | G | A | 1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+8568G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138494 | |||||||
chr12:108138504 | A | G | 2 | a0001c0001t0002g0141 a0002c0002t0002g0142 |
2 | HG04204.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-552+8578A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138504 | |||||||
chr12:108138523 | G | A | 4 | a0001c0001t0018g0031 a0001c0001t0026g0039 a0001c0001t0033g0037 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-552+8597G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138523 | |||||||
chr12:108138682 | C | G | 3 | a0001c0001t0059g0268 a0001c0001t0060g0267 a0001c0001t0061g0266 |
3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+8756C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138682 | |||||||
chr12:108138732 | C | T | 130 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(127): Show |
134 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-552+8806C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138732 | |||||||
chr12:108138800 | G | A | 1 | a0001c0001t0023g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-552+8874G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138800 | |||||||
chr12:108138915 | A | G | 4 | a0001c0001t0006g0088 a0001c0001t0008g0126 a0001c0003t0022g0236 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-552+8989A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138915 | |||||||
chr12:108139026 | G | A | 1 | a0006c0006t0016g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-552+9100G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139026 | |||||||
chr12:108139077 | A | G | 10 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0221 others(7): Show |
10 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-552+9151A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139077 | |||||||
chr12:108139086 | G | A | 6 | a0001c0001t0003g0130 a0002c0002t0001g0179 a0002c0002t0002g0181 others(3): Show |
6 | HG00423.hp1 HG00558.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.-552+9160G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139086 | |||||||
chr12:108139128 | A | G | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+9202A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139128 | |||||||
chr12:108139220 | T | G | 8 | a0001c0001t0007g0053 a0001c0001t0009g0052 a0001c0001t0054g0051 others(5): Show |
8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-552+9294T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139220 | |||||||
chr12:108139287 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-552+9361G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139287 | |||||||
chr12:108139447 | G | A | 1 | a0002c0002t0002g0142 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-552+9521G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139447 | |||||||
chr12:108139566 | C | A | 1 | a0001c0001t0056g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+9640C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139566 | |||||||
chr12:108139800 | A | C | 1 | a0001c0001t0049g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-552+9874A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139800 | |||||||
chr12:108139860 | G | A | 1 | a0001c0001t0056g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+9934G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139860 | |||||||
chr12:108139944 | A | C | 39 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(36): Show |
42 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.-552+10018A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139944 | |||||||
chr12:108140119 | G | A | 36 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(33): Show |
39 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.-552+10193G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108140119 | |||||||
chr12:108140210 | C | T | 1 | a0001c0001t0003g0103 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-552+10284C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108140210 | |||||||
chr12:108140262 | G | A | 15 | a0001c0001t0007g0053 a0001c0001t0009g0052 a0001c0001t0016g0269 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-552+10336G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108140262 | |||||||
chr12:108140285 | C | T | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+10359C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108140285 | |||||||
chr12:108140381 | C | T | 1 | a0002c0002t0001g0140 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-552+10455C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108140381 | |||||||
chr12:108140924 | C | T | 1 | a0001c0001t0012g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-552+10998C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108140924 | |||||||
chr12:108141025 | T | C | 1 | a0001c0001t0027g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-552+11099T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141025 | |||||||
chr12:108141080 | G | A | 1 | a0001c0001t0007g0034 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-552+11154G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141080 | |||||||
chr12:108141134 | G | A | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+11208G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141134 | |||||||
chr12:108141196 | A | G | 1 | a0001c0001t0010g0102 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-552+11270A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141196 | |||||||
chr12:108141238 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0003g0006 others(9): Show |
14 | HG01081.hp1 HG01175.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-552+11312G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141238 | |||||||
chr12:108141282 | G | A | 1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+11356G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141282 | |||||||
chr12:108141452 | A | C | 1 | a0001c0001t0003g0216 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-552+11526A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141452 | |||||||
chr12:108141536 | A | G | 204 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(201): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-552+11610A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141536 | |||||||
chr12:108141581 | G | A | 8 | a0001c0001t0007g0053 a0001c0001t0009g0052 a0001c0001t0054g0051 others(5): Show |
8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-552+11655G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141581 | |||||||
chr12:108141607 | G | A | 1 | a0001c0001t0002g0008 | 2 | HG02015.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-552+11681G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141607 | |||||||
chr12:108141777 | A | G | 16 | a0001c0001t0007g0053 a0001c0001t0009g0052 a0001c0001t0016g0269 others(13): Show |
16 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-552+11851A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141777 | |||||||
chr12:108141833 | A | G | 9 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0006g0088 others(6): Show |
9 | HG00642.hp2 HG01516.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-552+11907A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141833 | |||||||
chr12:108141872 | C | T | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+11946C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141872 | |||||||
chr12:108141915 | G | C | 8 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 others(5): Show |
8 | HG01943.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-552+11989G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141915 | |||||||
chr12:108142081 | C | T | 164 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(161): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-552+12155C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108142081 | |||||||
chr12:108142260 | T | C | 3 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 |
3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-552+12334T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108142260 | |||||||
chr12:108142553 | C | T | 1 | a0002c0002t0001g0140 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-552+12627C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108142553 | |||||||
chr12:108142729 | A | C | 1 | a0001c0001t0056g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+12803A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108142729 | |||||||
chr12:108142950 | G | A | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+13024G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108142950 | |||||||
chr12:108142983 | A | G | 1 | a0001c0001t0014g0139 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-552+13057A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108142983 | |||||||
chr12:108143010 | C | T | 3 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 |
3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-552+13084C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143010 | |||||||
chr12:108143128 | C | T | 1 | a0001c0001t0021g0256 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-552+13202C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143128 | |||||||
chr12:108143191 | A | G | 217 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(214): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.-552+13265A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143191 | |||||||
chr12:108143555 | T | C | 1 | a0001c0001t0021g0264 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-552+13629T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143555 | |||||||
chr12:108143837 | A | G | 1 | a0001c0001t0056g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+13911A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143837 | |||||||
chr12:108143848 | G | A | 1 | a0002c0002t0010g0182 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-552+13922G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143848 | |||||||
chr12:108143879 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-552+13953G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143879 | |||||||
chr12:108143893 | C | T | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+13967C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143893 | |||||||
chr12:108143933 | C | A | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+14007C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143933 | |||||||
chr12:108144010 | C | T | 1 | a0001c0001t0003g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-552+14084C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144010 | |||||||
chr12:108144218 | C | T | 5 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0011g0092 others(2): Show |
5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+14292C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144218 | |||||||
chr12:108144250 | G | A | 2 | a0001c0001t0030g0127 a0001c0001t0049g0128 |
2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-552+14324G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144250 | |||||||
chr12:108144271 | G | T | 1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+14345G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144271 | |||||||
chr12:108144282 | G | A | 165 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(162): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-552+14356G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144282 | |||||||
chr12:108144390 | C | T | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+14464C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144390 | |||||||
chr12:108144419 | A | T | 3 | a0001c0001t0008g0086 a0001c0001t0008g0113 a0001c0001t0008g0154 |
3 | HG01884.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-552+14493A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144419 | |||||||
chr12:108144424 | T | C | 1 | a0001c0001t0056g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+14498T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144424 | |||||||
chr12:108144524 | A | G | 180 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(177): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-552+14598A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144524 | |||||||
chr12:108144667 | T | A | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+14741T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144667 | |||||||
chr12:108144786 | A | G | 1 | a0001c0001t0020g0085 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-552+14860A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144786 | |||||||
chr12:108145054 | C | A | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+15128C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108145054 | |||||||
chr12:108145215 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-552+15289C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108145215 | |||||||
chr12:108145501 | C | T | 180 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(177): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-552+15575C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108145501 | |||||||
chr12:108145502 | G | A | 9 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0006g0088 others(6): Show |
9 | HG00642.hp2 HG01516.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-552+15576G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108145502 | |||||||
chr12:108145996 | G | A | 1 | a0001c0001t0027g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-552+16070G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108145996 | |||||||
chr12:108146334 | C | T | 166 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(163): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-552+16408C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146334 | |||||||
chr12:108146588 | G | A | 19 | a0001c0001t0007g0002 a0001c0001t0007g0016 a0001c0001t0007g0017 others(16): Show |
20 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.-552+16662G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146588 | |||||||
chr12:108146666 | G | A | 1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+16740G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146666 | |||||||
chr12:108146710 | G | A | 5 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0011g0092 others(2): Show |
5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+16784G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146710 | |||||||
chr12:108146809 | C | T | 164 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(161): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-552+16883C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146809 | |||||||
chr12:108146840 | A | G | 5 | a0001c0001t0023g0146 a0001c0001t0030g0127 a0001c0001t0042g0223 others(2): Show |
5 | HG02630.hp1 HG02717.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+16914A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146840 | |||||||
chr12:108146856 | G | T | 3 | a0001c0001t0015g0228 a0001c0001t0029g0226 a0001c0001t0029g0227 |
3 | HG01099.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-552+16930G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146856 | |||||||
chr12:108146987 | G | C | 1 | a0001c0001t0036g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-552+17061G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146987 | |||||||
chr12:108147051 | G | T | 1 | a0002c0002t0002g0215 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-552+17125G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147051 | |||||||
chr12:108147100 | G | A | 1 | a0001c0001t0062g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-552+17174G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147100 | |||||||
chr12:108147476 | G | A | 1 | a0001c0003t0037g0065 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-552+17550G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147476 | |||||||
chr12:108147580 | C | T | 1 | a0001c0001t0012g0036 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-552+17654C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147580 | |||||||
chr12:108147598 | C | T | 3 | a0001c0001t0001g0243 a0001c0001t0003g0244 a0002c0002t0010g0214 |
3 | HG02080.hp1 NA19000.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-552+17672C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147598 | |||||||
chr12:108147635 | G | T | 3 | a0001c0001t0003g0263 a0002c0002t0003g0242 a0002c0002t0003g0259 |
3 | HG00280.hp2 HG01261.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-552+17709G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147635 | |||||||
chr12:108147689 | CA | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0002c0002t0019g0083 |
3 | HG00733.hp1 HG00735.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-552+17765delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108147689 | ||||||
chr12:108147691 | A | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0002c0002t0019g0083 |
3 | HG00733.hp1 HG00735.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-552+17765A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147691 | |||||||
chr12:108147692 | T | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0002c0002t0019g0083 |
3 | HG00733.hp1 HG00735.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-552+17766T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147692 | |||||||
chr12:108147857 | A | G | 2 | a0001c0001t0017g0212 a0001c0001t0017g0213 |
2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-552+17931A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147857 | |||||||
chr12:108147993 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-552+18067G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147993 | |||||||
chr12:108148109 | C | T | 2 | a0001c0001t0016g0269 a0001c0001t0056g0265 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+18183C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148109 | |||||||
chr12:108148277 | G | A | 5 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0011g0092 others(2): Show |
5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+18351G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148277 | |||||||
chr12:108148352 | C | A | 1 | a0001c0001t0061g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-552+18426C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148352 | |||||||
chr12:108148447 | T | C | 1 | a0002c0002t0010g0237 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-552+18521T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148447 | |||||||
chr12:108148458 | C | T | 1 | a0001c0001t0056g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+18532C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148458 | |||||||
chr12:108148667 | G | T | 1 | a0001c0001t0002g0137 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-552+18741G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148667 | |||||||
chr12:108148787 | T | C | 4 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 others(1): Show |
5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+18861T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148787 | |||||||
chr12:108148814 | C | A | 163 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(160): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.-552+18888C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148814 | |||||||
chr12:108148956 | C | T | 4 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0012g0032 others(1): Show |
4 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.-552+19030C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148956 | |||||||
chr12:108148975 | A | G | 2 | a0001c0001t0016g0269 a0001c0001t0056g0265 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+19049A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148975 | |||||||
chr12:108149047 | A | G | 12 | a0001c0001t0007g0034 a0001c0001t0009g0003 a0001c0001t0009g0043 others(9): Show |
14 | HG00099.hp2 HG01069.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.-552+19121A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149047 | |||||||
chr12:108149080 | T | C | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+19154T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149080 | |||||||
chr12:108149222 | G | A | 1 | a0001c0001t0061g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-552+19296G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149222 | |||||||
chr12:108149360 | A | G | 2 | a0001c0001t0016g0269 a0001c0001t0056g0265 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+19434A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149360 | |||||||
chr12:108149489 | A | G | 1 | a0001c0001t0056g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+19563A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149489 | |||||||
chr12:108149571 | TGCTCAG | T | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+19648_-552+19 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108149571 | ||||||
chr12:108149675 | C | T | 1 | a0001c0001t0056g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+19749C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149675 | |||||||
chr12:108149746 | T | A | 5 | a0001c0001t0034g0224 a0001c0001t0034g0250 a0001c0001t0035g0070 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+19820T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149746 | |||||||
chr12:108149805 | T | A | 235 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(232): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.-552+19879T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149805 | |||||||
chr12:108149825 | G | A | 1 | a0001c0001t0043g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-552+19899G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149825 | |||||||
chr12:108149852 | C | G | 9 | a0001c0001t0009g0052 a0001c0001t0016g0269 a0001c0001t0034g0224 others(6): Show |
9 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-552+19926C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149852 | |||||||
chr12:108149988 | G | T | 3 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 |
3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-552+20062G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149988 | |||||||
chr12:108150118 | AGGGT | A | 4 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 others(1): Show |
5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+20195_-552+20 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108150118 | ||||||
chr12:108150172 | A | T | 2 | a0001c0001t0007g0053 a0001c0003t0012g0049 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-552+20246A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150172 | |||||||
chr12:108150188 | G | A | 1 | a0002c0002t0002g0222 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-552+20262G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150188 | |||||||
chr12:108150211 | G | A | 1 | a0001c0001t0003g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-552+20285G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150211 | |||||||
chr12:108150212 | A | G | 1 | a0001c0001t0003g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-552+20286A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150212 | |||||||
chr12:108150214 | C | A | 1 | a0001c0001t0003g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-552+20288C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150214 | |||||||
chr12:108150379 | G | A | 1 | a0001c0001t0056g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+20453G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150379 | |||||||
chr12:108150598 | G | A | 1 | a0001c0001t0024g0025 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-552+20672G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150598 | |||||||
chr12:108150669 | C | T | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-552+20743C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150669 | |||||||
chr12:108150878 | C | G | 6 | a0001c0001t0017g0094 a0001c0001t0017g0095 a0001c0001t0017g0096 others(3): Show |
6 | HG00323.hp2 HG01167.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-552+20952C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150878 | |||||||
chr12:108150964 | G | C | 1 | a0001c0001t0007g0026 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-552+21038G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150964 | |||||||
chr12:108150991 | C | T | 1 | a0002c0002t0010g0182 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-552+21065C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150991 | |||||||
chr12:108151283 | C | T | 5 | a0001c0001t0007g0053 a0001c0001t0023g0146 a0001c0001t0042g0223 others(2): Show |
5 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+21357C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151283 | |||||||
chr12:108151353 | C | T | 1 | a0001c0001t0023g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-552+21427C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151353 | |||||||
chr12:108151461 | G | T | 2 | a0001c0001t0003g0138 a0002c0002t0002g0222 |
2 | NA18981.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-552+21535G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151461 | |||||||
chr12:108151488 | G | A | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-552+21562G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151488 | |||||||
chr12:108151611 | T | C | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-552+21685T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151611 | |||||||
chr12:108151707 | C | A | 5 | a0001c0001t0007g0053 a0001c0001t0023g0146 a0001c0001t0042g0223 others(2): Show |
5 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+21781C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151707 | |||||||
chr12:108151849 | A | G | 1 | a0002c0002t0001g0211 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-552+21923A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151849 | |||||||
chr12:108151960 | G | A | 4 | a0001c0001t0012g0033 a0001c0001t0012g0036 a0001c0001t0012g0044 others(1): Show |
4 | HG01943.hp1 HG02683.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-552+22034G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151960 | |||||||
chr12:108152013 | C | T | 1 | a0001c0001t0004g0173 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-552+22087C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152013 | |||||||
chr12:108152014 | G | A | 4 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 others(1): Show |
5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+22088G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152014 | |||||||
chr12:108152102 | G | A | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-552+22176G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152102 | |||||||
chr12:108152103 | A | G | 194 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(191): Show |
201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-552+22177A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152103 | |||||||
chr12:108152208 | A | C | 80 | a0001c0001t0001g0081 a0001c0001t0001g0133 a0001c0001t0001g0149 others(77): Show |
81 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-552+22282A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152208 | |||||||
chr12:108152292 | A | G | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-552+22366A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152292 | |||||||
chr12:108152582 | G | A | 3 | a0001c0003t0016g0059 a0001c0003t0031g0054 a0001c0003t0031g0055 |
3 | HG01243.hp2 HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-552+22656G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152582 | |||||||
chr12:108152734 | A | G | 1 | a0001c0001t0005g0255 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-552+22808A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152734 | |||||||
chr12:108152741 | T | C | 1 | a0001c0001t0012g0032 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-552+22815T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152741 | |||||||
chr12:108152761 | A | C | 1 | a0001c0001t0009g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-552+22835A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152761 | |||||||
chr12:108152762 | C | T | 1 | a0001c0001t0014g0148 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-552+22836C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152762 | |||||||
chr12:108152766 | G | A | 157 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(154): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-552+22840G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152766 | |||||||
chr12:108152824 | C | G | 9 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0006g0088 others(6): Show |
9 | HG00642.hp2 HG01516.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-552+22898C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152824 | |||||||
chr12:108153015 | A | T | 12 | a0001c0001t0007g0053 a0001c0001t0023g0146 a0001c0001t0030g0127 others(9): Show |
12 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-552+23089A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153015 | |||||||
chr12:108153101 | T | TCAAA | 14 | a0001c0001t0001g0075 a0001c0001t0002g0174 a0001c0001t0009g0003 others(11): Show |
16 | HG00140.hp1 HG01168.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-552+23200_-552+23 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108153101 | ||||||
chr12:108153101 | T | TCAAACAA others(1): Show |
59 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.-552+23196_-552+23 others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108153101 | ||||||
chr12:108153101 | T | TCAAACAA others(5): Show |
83 | a0001c0001t0001g0005 a0001c0001t0001g0133 a0001c0001t0001g0143 others(80): Show |
85 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-552+23192_-552+23 others(18): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108153101 | ||||||
chr12:108153101 | T | TCAAACAA others(9): Show |
5 | a0001c0001t0009g0043 a0001c0001t0025g0035 a0001c0001t0025g0046 others(2): Show |
5 | HG03239.hp1 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.-552+23188_-552+23 others(22): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108153101 | ||||||
chr12:108153101 | TCAAA | T | 13 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0006g0088 others(10): Show |
13 | HG00642.hp2 HG01243.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.-552+23200_-552+23 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108153101 | ||||||
chr12:108153418 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-552+23492T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153418 | |||||||
chr12:108153462 | G | A | 1 | a0001c0001t0017g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-552+23536G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153462 | |||||||
chr12:108153569 | T | C | 3 | a0001c0001t0059g0268 a0001c0001t0060g0267 a0001c0001t0061g0266 |
3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+23643T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153569 | |||||||
chr12:108153587 | A | G | 193 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(190): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-552+23661A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153587 | |||||||
chr12:108153619 | C | T | 5 | a0001c0001t0002g0079 a0001c0001t0002g0141 a0001c0001t0003g0103 others(2): Show |
5 | HG00597.hp2 HG04204.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+23693C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153619 | |||||||
chr12:108153844 | C | T | 1 | a0004c0007t0024g0028 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-552+23918C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153844 | |||||||
chr12:108153966 | G | A | 1 | a0001c0001t0003g0067 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-552+24040G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153966 | |||||||
chr12:108154020 | G | A | 1 | a0002c0002t0003g0191 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-552+24094G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154020 | |||||||
chr12:108154057 | A | G | 193 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(190): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-552+24131A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154057 | |||||||
chr12:108154125 | G | A | 191 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(188): Show |
198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.-552+24199G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154125 | |||||||
chr12:108154151 | T | A | 1 | a0001c0001t0002g0192 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-552+24225T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154151 | |||||||
chr12:108154208 | C | A | 12 | a0001c0001t0007g0053 a0001c0001t0023g0146 a0001c0001t0030g0127 others(9): Show |
12 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-552+24282C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154208 | |||||||
chr12:108154242 | G | T | 181 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(178): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.-552+24316G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154242 | |||||||
chr12:108154387 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-552+24461G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154387 | |||||||
chr12:108154451 | C | T | 1 | a0002c0002t0002g0209 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-552+24525C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154451 | |||||||
chr12:108154513 | T | C | 193 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(190): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-552+24587T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154513 | |||||||
chr12:108154768 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-552+24842A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154768 | |||||||
chr12:108154898 | A | G | 12 | a0001c0001t0007g0053 a0001c0001t0023g0146 a0001c0001t0030g0127 others(9): Show |
12 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-552+24972A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154898 | |||||||
chr12:108155009 | G | A | 1 | a0001c0001t0033g0037 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-552+25083G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108155009 | |||||||
chr12:108155139 | C | A | 4 | a0001c0001t0007g0053 a0001c0001t0042g0223 a0001c0001t0043g0147 others(1): Show |
4 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+25213C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108155139 | |||||||
chr12:108155147 | A | C | 193 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(190): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-552+25221A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108155147 | |||||||
chr12:108155155 | C | T | 191 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(188): Show |
198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.-552+25229C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108155155 | |||||||
chr12:108155320 | C | G | 157 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(154): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-552+25394C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108155320 | |||||||
chr12:108155373 | C | T | 2 | a0001c0001t0032g0004 a0001c0001t0058g0040 |
3 | HG00099.hp2 HG01257.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-552+25447C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108155373 | |||||||
chr12:108156098 | G | A | 1 | a0002c0002t0001g0211 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-552+26172G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156098 | |||||||
chr12:108156131 | C | T | 1 | a0001c0001t0008g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-552+26205C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156131 | |||||||
chr12:108156190 | C | T | 2 | a0001c0001t0007g0053 a0001c0003t0012g0049 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-552+26264C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156190 | |||||||
chr12:108156212 | G | A | 1 | a0001c0001t0005g0158 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-552+26286G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156212 | |||||||
chr12:108156402 | A | G | 1 | a0001c0001t0026g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-552+26476A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156402 | |||||||
chr12:108156539 | G | A | 12 | a0001c0001t0005g0090 a0001c0001t0006g0088 a0001c0001t0008g0126 others(9): Show |
12 | HG00642.hp2 HG01243.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.-552+26613G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156539 | |||||||
chr12:108156598 | T | A | 1 | a0001c0001t0001g0243 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-552+26672T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156598 | |||||||
chr12:108156659 | A | G | 1 | a0001c0001t0019g0208 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-552+26733A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156659 | |||||||
chr12:108157024 | C | T | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+27098C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157024 | |||||||
chr12:108157084 | G | A | 6 | a0001c0003t0016g0059 a0001c0003t0022g0236 a0001c0003t0022g0257 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-552+27158G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157084 | |||||||
chr12:108157126 | T | C | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-552+27200T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157126 | |||||||
chr12:108157140 | T | C | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+27214T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157140 | |||||||
chr12:108157149 | A | G | 13 | a0001c0001t0007g0053 a0001c0001t0016g0269 a0001c0001t0023g0146 others(10): Show |
13 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.-552+27223A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157149 | |||||||
chr12:108157210 | C | G | 3 | a0001c0001t0059g0268 a0001c0001t0060g0267 a0001c0001t0061g0266 |
3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+27284C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157210 | |||||||
chr12:108157216 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-552+27290A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157216 | |||||||
chr12:108157547 | T | C | 15 | a0001c0001t0003g0006 a0001c0001t0003g0066 a0001c0001t0003g0067 others(12): Show |
17 | HG01081.hp1 HG01175.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-552+27621T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157547 | |||||||
chr12:108157653 | G | A | 10 | a0001c0001t0007g0053 a0001c0001t0023g0146 a0001c0001t0042g0223 others(7): Show |
10 | HG02109.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-552+27727G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157653 | |||||||
chr12:108158199 | G | A | 11 | a0001c0001t0007g0053 a0001c0001t0016g0269 a0001c0001t0023g0146 others(8): Show |
11 | HG02109.hp2 HG02717.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-552+28273G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108158199 | |||||||
chr12:108158256 | C | T | 1 | a0001c0001t0021g0256 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-552+28330C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108158256 | |||||||
chr12:108158278 | C | T | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-552+28352C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108158278 | |||||||
chr12:108158787 | G | A | 1 | a0006c0006t0016g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-552+28861G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108158787 | |||||||
chr12:108158805 | A | G | 13 | a0001c0001t0007g0053 a0001c0001t0016g0269 a0001c0001t0023g0146 others(10): Show |
13 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.-552+28879A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108158805 | |||||||
chr12:108159147 | T | A | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+29221T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159147 | |||||||
chr12:108159152 | C | A | 2 | a0001c0003t0031g0054 a0001c0003t0031g0055 |
2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-552+29226C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159152 | |||||||
chr12:108159299 | G | A | 1 | a0001c0001t0017g0094 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-552+29373G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159299 | |||||||
chr12:108159402 | C | T | 1 | a0002c0002t0002g0207 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-552+29476C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159402 | |||||||
chr12:108159418 | G | A | 2 | a0001c0001t0005g0115 a0001c0001t0005g0116 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-552+29492G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159418 | |||||||
chr12:108159461 | A | G | 1 | a0002c0002t0001g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-552+29535A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159461 | |||||||
chr12:108159502 | C | T | 3 | a0001c0001t0013g0204 a0002c0002t0001g0203 a0002c0002t0064g0205 |
3 | HG00639.hp1 HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-552+29576C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159502 | |||||||
chr12:108159504 | G | A | 3 | a0001c0001t0004g0114 a0001c0001t0021g0159 a0001c0010t0046g0230 |
3 | HG01981.hp2 HG02735.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-552+29578G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159504 | |||||||
chr12:108159537 | G | T | 4 | a0001c0001t0005g0090 a0001c0001t0011g0092 a0001c0001t0015g0089 others(1): Show |
4 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+29611G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159537 | |||||||
chr12:108159609 | T | A | 6 | a0001c0003t0016g0059 a0001c0003t0022g0236 a0001c0003t0022g0257 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-552+29683T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159609 | |||||||
chr12:108159728 | G | A | 1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+29802G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159728 | |||||||
chr12:108159836 | G | T | 1 | a0002c0002t0010g0214 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-552+29910G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159836 | |||||||
chr12:108159882 | C | T | 3 | a0001c0001t0059g0268 a0001c0001t0060g0267 a0001c0001t0061g0266 |
3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+29956C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159882 | |||||||
chr12:108159903 | G | A | 10 | a0001c0001t0007g0053 a0001c0001t0023g0146 a0001c0001t0042g0223 others(7): Show |
10 | HG02109.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-552+29977G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159903 | |||||||
chr12:108159989 | T | C | 2 | a0001c0001t0007g0053 a0001c0003t0012g0049 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-552+30063T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159989 | |||||||
chr12:108160052 | A | G | 1 | a0001c0001t0019g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-552+30126A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108160052 | |||||||
chr12:108160272 | T | G | 1 | a0001c0001t0015g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-552+30346T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108160272 | |||||||
chr12:108160350 | A | G | 12 | a0001c0001t0007g0053 a0001c0001t0023g0146 a0001c0001t0030g0127 others(9): Show |
12 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-552+30424A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108160350 | |||||||
chr12:108160649 | C | A | 1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+30723C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108160649 | |||||||
chr12:108161342 | T | C | 160 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(157): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.-552+31416T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108161342 | |||||||
chr12:108161465 | G | A | 1 | a0001c0001t0028g0231 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-552+31539G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108161465 | |||||||
chr12:108161481 | G | A | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-552+31555G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108161481 | |||||||
chr12:108161637 | A | G | 1 | a0001c0001t0011g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-552+31711A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108161637 | |||||||
chr12:108161773 | T | C | 2 | a0001c0001t0002g0193 a0001c0001t0003g0216 |
2 | HG02523.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.-552+31847T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108161773 | |||||||
chr12:108162062 | A | G | 195 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(192): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.-552+32136A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162062 | |||||||
chr12:108162129 | G | A | 1 | a0002c0002t0001g0194 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-552+32203G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162129 | |||||||
chr12:108162435 | T | G | 157 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(154): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-552+32509T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162435 | |||||||
chr12:108162514 | C | T | 1 | a0002c0002t0002g0222 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-552+32588C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162514 | |||||||
chr12:108162624 | G | A | 1 | a0001c0001t0023g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-551-32658G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162624 | |||||||
chr12:108162649 | G | A | 77 | a0001c0001t0001g0133 a0001c0001t0001g0149 a0001c0001t0001g0176 others(74): Show |
78 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-551-32633G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162649 | |||||||
chr12:108162838 | T | G | 1 | a0001c0001t0038g0184 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-551-32444T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162838 | |||||||
chr12:108162900 | T | G | 1 | a0004c0007t0024g0028 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-551-32382T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162900 | |||||||
chr12:108163134 | T | C | 4 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 others(1): Show |
5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-551-32148T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163134 | |||||||
chr12:108163143 | G | A | 1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-551-32139G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163143 | |||||||
chr12:108163450 | A | G | 12 | a0001c0001t0007g0053 a0001c0001t0023g0146 a0001c0001t0030g0127 others(9): Show |
12 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-551-31832A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163450 | |||||||
chr12:108163556 | C | A | 4 | a0001c0001t0006g0117 a0001c0001t0006g0160 a0001c0001t0006g0161 others(1): Show |
4 | HG00735.hp2 HG01361.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-31726C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163556 | |||||||
chr12:108163558 | T | C | 1 | a0002c0002t0010g0195 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-551-31724T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163558 | |||||||
chr12:108163605 | G | A | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-31677G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163605 | |||||||
chr12:108163609 | G | A | 157 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(154): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-551-31673G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163609 | |||||||
chr12:108163644 | T | A | 1 | a0002c0002t0001g0203 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-551-31638T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163644 | |||||||
chr12:108163712 | A | G | 8 | a0001c0001t0003g0006 a0001c0001t0003g0066 a0001c0001t0003g0067 others(5): Show |
9 | HG01081.hp1 HG01175.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-551-31570A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163712 | |||||||
chr12:108163853 | G | GT | 12 | a0001c0001t0007g0053 a0001c0001t0023g0146 a0001c0001t0030g0127 others(9): Show |
12 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-551-31422dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108163853 | ||||||
chr12:108164009 | TGATGGCT others(8): Show |
T | 1 | a0001c0001t0003g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-551-31272_-551-31 others(21): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164009 | |||||||
chr12:108164137 | TC | T | 7 | a0001c0001t0004g0114 a0001c0001t0004g0164 a0001c0001t0004g0173 others(4): Show |
7 | HG01167.hp2 HG01257.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-31143delC | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108164137 | ||||||
chr12:108164138 | C | CT | 11 | a0001c0001t0002g0137 a0001c0001t0002g0201 a0001c0001t0004g0112 others(8): Show |
11 | HG01361.hp1 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(7): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTT | 5 | a0001c0001t0002g0193 a0001c0001t0003g0216 a0001c0001t0003g0258 others(2): Show |
5 | HG00597.hp1 HG02523.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTTTTTT | 3 | a0001c0001t0007g0053 a0001c0001t0013g0247 a0001c0003t0012g0049 |
3 | HG02723.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0081 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-551-31144_-551-31 others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0007g0016 a0001c0001t0059g0268 a0001c0001t0061g0266 |
3 | HG02970.hp1 NA18906.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(17): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTTTTTTT others(6): Show |
17 | a0001c0001t0001g0005 a0001c0001t0001g0084 a0001c0001t0001g0098 others(14): Show |
18 | HG00597.hp2 HG00733.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(19): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTTTTTTT others(7): Show |
16 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(13): Show |
16 | HG00280.hp1 HG01168.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(20): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTTTTTTT others(8): Show |
22 | a0001c0001t0001g0082 a0001c0001t0001g0143 a0001c0001t0001g0149 others(19): Show |
22 | HG00609.hp1 HG00609.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(21): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTTTTTTT others(9): Show |
46 | a0001c0001t0001g0144 a0001c0001t0001g0177 a0001c0001t0001g0202 others(43): Show |
47 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(22): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTTTTTTT others(10): Show |
31 | a0001c0001t0001g0133 a0001c0001t0001g0243 a0001c0001t0002g0192 others(28): Show |
31 | HG00438.hp1 HG00738.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(23): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTTTTTTT others(11): Show |
10 | a0001c0001t0001g0218 a0001c0001t0003g0263 a0001c0001t0004g0225 others(7): Show |
10 | HG01261.hp1 HG01358.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(24): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTTTTTTT others(12): Show |
3 | a0001c0001t0001g0221 a0001c0001t0010g0189 a0002c0002t0003g0240 |
3 | HG00438.hp2 HG01175.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(25): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0017g0094 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-551-31144_-551-31 others(26): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | C | CTTTTTTT others(15): Show |
2 | a0001c0001t0069g0136 a0002c0002t0003g0242 |
2 | HG00280.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(28): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | CCT | C | 21 | a0001c0001t0003g0006 a0001c0001t0003g0066 a0001c0001t0003g0067 others(18): Show |
23 | HG00099.hp1 HG01081.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.-551-31143_-551-31 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | CCTT | C | 7 | a0001c0001t0003g0068 a0001c0001t0016g0269 a0001c0001t0027g0013 others(4): Show |
8 | HG02109.hp2 HG02723.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-551-31143_-551-31 others(9): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | CCTTTTT | C | 3 | a0001c0003t0016g0059 a0001c0003t0031g0054 a0001c0003t0031g0055 |
3 | HG01243.hp2 HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-551-31143_-551-31 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | CCTTTTTT | C | 3 | a0001c0003t0022g0236 a0001c0003t0022g0257 a0006c0006t0016g0050 |
3 | HG02615.hp1 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-551-31143_-551-31 others(13): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164138 | CCTTTTTT others(3): Show |
C | 7 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0006g0088 others(4): Show |
7 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-31143_-551-31 others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | |||||||
chr12:108164139 | C | T | 222 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(219): Show |
230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.-551-31143C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164139 | |||||||
chr12:108164162 | T | TTTTTTTT others(7): Show |
1 | a0001c0001t0020g0085 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-551-31120_-551-31 others(20): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164162 | |||||||
chr12:108164567 | A | G | 2 | a0002c0002t0001g0190 a0002c0002t0018g0042 |
2 | HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-551-30715A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164567 | |||||||
chr12:108164617 | C | G | 1 | a0001c0001t0012g0036 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-551-30665C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164617 | |||||||
chr12:108164908 | G | A | 1 | a0001c0003t0037g0065 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-551-30374G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164908 | |||||||
chr12:108165045 | G | A | 1 | a0003c0004t0026g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-551-30237G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108165045 | |||||||
chr12:108165123 | G | T | 3 | a0001c0001t0059g0268 a0001c0001t0060g0267 a0001c0001t0061g0266 |
3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-551-30159G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108165123 | |||||||
chr12:108165139 | G | T | 25 | a0001c0001t0003g0006 a0001c0001t0003g0066 a0001c0001t0003g0067 others(22): Show |
27 | HG00642.hp2 HG01081.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.-551-30143G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108165139 | |||||||
chr12:108165680 | C | T | 148 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(145): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-551-29602C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108165680 | |||||||
chr12:108165986 | T | G | 1 | a0001c0001t0006g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-551-29296T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108165986 | |||||||
chr12:108166099 | T | C | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-551-29183T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166099 | |||||||
chr12:108166331 | A | G | 1 | a0001c0001t0023g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-551-28951A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166331 | |||||||
chr12:108166550 | G | A | 155 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(152): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-551-28732G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166550 | |||||||
chr12:108166716 | C | T | 168 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(165): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-551-28566C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166716 | |||||||
chr12:108166724 | T | TCTCTTCT others(11): Show |
1 | a0001c0001t0002g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-551-28558_-551-28 others(24): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166724 | |||||||
chr12:108166726 | C | T | 1 | a0001c0001t0002g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-551-28556C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166726 | |||||||
chr12:108166741 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-551-28541T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166741 | |||||||
chr12:108166745 | C | CTTCTTCT others(8): Show |
1 | a0002c0002t0001g0196 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-551-28532_-551-28 others(21): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166745 | ||||||
chr12:108166745 | C | CTTCTTTC others(3): Show |
1 | a0002c0002t0010g0214 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-551-28529_-551-28 others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166745 | ||||||
chr12:108166745 | C | CTTTCTTT others(10): Show |
1 | a0001c0001t0065g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-551-28535_-551-28 others(23): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166745 | ||||||
chr12:108166745 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0002g0141 a0001c0001t0007g0017 |
3 | HG01243.hp1 NA18960.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-551-28537C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166745 | |||||||
chr12:108166745 | CTTCTTTC others(10): Show |
C | 5 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0011g0092 others(2): Show |
5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-551-28518_-551-28 others(23): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166745 | ||||||
chr12:108166746 | T | TTCTTTC | 2 | a0001c0001t0001g0243 a0001c0001t0003g0244 |
2 | NA19000.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-551-28534_-551-28 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166746 | ||||||
chr12:108166748 | CTTTCTTT others(6): Show |
C | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-28518_-551-28 others(19): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166748 | ||||||
chr12:108166756 | CTTTCT | C | 5 | a0001c0001t0006g0088 a0001c0001t0008g0126 a0001c0001t0010g0189 others(2): Show |
5 | HG00438.hp2 HG01433.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-28518_-551-28 others(11): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166756 | ||||||
chr12:108166760 | C | T | 2 | a0001c0001t0007g0002 a0001c0001t0007g0016 |
3 | NA18944.hp1 NA18952.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-551-28522C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166760 | |||||||
chr12:108166760 | CT | C | 15 | a0001c0001t0001g0075 a0001c0001t0001g0133 a0001c0001t0007g0026 others(12): Show |
16 | HG00438.hp1 HG01168.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.-551-28518delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166760 | ||||||
chr12:108166761 | T | TCTTTCTT others(2): Show |
2 | a0001c0001t0007g0002 a0001c0001t0007g0016 |
3 | NA18944.hp1 NA18952.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-551-28521_-551-28 others(15): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166761 | |||||||
chr12:108166761 | T | TTTC | 20 | a0001c0001t0001g0186 a0001c0001t0001g0243 a0001c0001t0002g0071 others(17): Show |
20 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(9): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTCTTTC | 22 | a0001c0001t0001g0076 a0001c0001t0001g0107 a0001c0001t0001g0149 others(19): Show |
22 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(13): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTCTTTC others(22): Show |
1 | a0001c0001t0027g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(35): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTCTTTC others(4): Show |
38 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0177 others(35): Show |
38 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(17): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTCTTTC others(8): Show |
36 | a0001c0001t0001g0082 a0001c0001t0001g0143 a0001c0001t0001g0144 others(33): Show |
36 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(21): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTCTTTC others(12): Show |
19 | a0001c0001t0001g0005 a0001c0001t0001g0176 a0001c0001t0002g0104 others(16): Show |
20 | HG00558.hp1 HG00639.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(25): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTCTTTC others(16): Show |
8 | a0001c0001t0002g0137 a0001c0001t0009g0015 a0001c0001t0049g0128 others(5): Show |
8 | HG01081.hp2 HG02148.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(29): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTCTTTC others(20): Show |
8 | a0001c0001t0002g0008 a0001c0001t0002g0192 a0001c0001t0003g0138 others(5): Show |
8 | HG01943.hp2 HG02109.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(33): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTCTTTC others(24): Show |
4 | a0001c0001t0002g0008 a0001c0001t0002g0077 a0001c0001t0009g0052 others(1): Show |
4 | HG01109.hp1 HG02015.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(37): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTTC | 5 | a0001c0001t0004g0109 a0001c0001t0006g0117 a0001c0001t0006g0160 others(2): Show |
5 | HG00735.hp2 HG01361.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-551-28495_-551-28 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTTTCTT others(10): Show |
1 | a0001c0001t0061g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-551-28518_-551-28 others(23): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTTTCTT others(14): Show |
1 | a0001c0003t0022g0257 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-551-28518_-551-28 others(27): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTTTCTT others(18): Show |
1 | a0001c0003t0031g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-551-28518_-551-28 others(31): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTTTCTT others(22): Show |
4 | a0001c0001t0016g0269 a0001c0003t0022g0236 a0001c0003t0031g0054 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-28518_-551-28 others(35): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | T | TTTTTCTT others(30): Show |
1 | a0001c0003t0016g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-551-28518_-551-28 others(43): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166761 | TTTTC | T | 3 | a0001c0001t0003g0239 a0001c0001t0004g0163 a0001c0001t0006g0001 |
3 | HG00099.hp1 NA18906.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.-551-28495_-551-28 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | ||||||
chr12:108166787 | T | G | 1 | a0001c0001t0034g0250 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-551-28495T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166787 | |||||||
chr12:108166791 | G | GTCTT | 5 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0019g0061 others(2): Show |
6 | HG01884.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-551-28479_-551-28 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166791 | ||||||
chr12:108166791 | G | T | 5 | a0001c0001t0009g0052 a0001c0001t0027g0013 a0001c0001t0059g0268 others(2): Show |
6 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-551-28491G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166791 | |||||||
chr12:108166805 | C | CTT | 3 | a0001c0001t0027g0013 a0001c0001t0060g0267 a0001c0001t0061g0266 |
4 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-28476_-551-28 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166805 | ||||||
chr12:108166805 | C | CTTTCTTT others(19): Show |
1 | a0001c0001t0059g0268 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-551-28476_-551-28 others(32): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166805 | ||||||
chr12:108166807 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-551-28475C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166807 | |||||||
chr12:108166811 | T | G | 1 | a0002c0002t0001g0197 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-551-28471T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166811 | |||||||
chr12:108166817 | C | CT | 6 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0011g0092 others(3): Show |
6 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-551-28451dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166817 | ||||||
chr12:108166851 | G | A | 1 | a0001c0001t0023g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-551-28431G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166851 | |||||||
chr12:108166873 | A | G | 183 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(180): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.-551-28409A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166873 | |||||||
chr12:108166890 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-551-28392C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166890 | |||||||
chr12:108166905 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-551-28377G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166905 | |||||||
chr12:108167153 | G | T | 11 | a0001c0001t0016g0269 a0001c0001t0027g0013 a0001c0001t0059g0268 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-551-28129G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108167153 | |||||||
chr12:108167167 | C | T | 1 | a0001c0001t0045g0172 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-551-28115C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108167167 | |||||||
chr12:108167358 | T | G | 2 | a0001c0001t0019g0061 a0001c0001t0019g0062 |
2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-551-27924T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108167358 | |||||||
chr12:108167413 | A | G | 1 | a0002c0002t0037g0078 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-551-27869A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108167413 | |||||||
chr12:108167653 | C | T | 8 | a0001c0001t0005g0072 a0001c0001t0005g0171 a0001c0001t0006g0007 others(5): Show |
9 | NA18940.hp1 NA18948.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-551-27629C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108167653 | |||||||
chr12:108167946 | G | A | 4 | a0001c0001t0018g0031 a0001c0001t0026g0039 a0001c0001t0033g0037 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-27336G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108167946 | |||||||
chr12:108168003 | A | T | 1 | a0001c0001t0023g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-551-27279A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168003 | |||||||
chr12:108168193 | T | A | 1 | a0002c0002t0013g0187 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-551-27089T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168193 | |||||||
chr12:108168197 | G | A | 1 | a0001c0001t0021g0256 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-551-27085G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168197 | |||||||
chr12:108168490 | G | C | 1 | a0002c0009t0001g0178 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-551-26792G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168490 | |||||||
chr12:108168533 | CACTT | C | 155 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(152): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-551-26741_-551-26 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108168533 | ||||||
chr12:108168626 | A | G | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-26656A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168626 | |||||||
chr12:108168684 | G | T | 4 | a0001c0001t0012g0033 a0001c0001t0012g0036 a0001c0001t0012g0044 others(1): Show |
4 | HG01943.hp1 HG02683.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-26598G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168684 | |||||||
chr12:108168774 | A | G | 2 | a0001c0001t0007g0053 a0001c0003t0012g0049 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-551-26508A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168774 | |||||||
chr12:108169056 | A | T | 4 | a0001c0001t0006g0088 a0001c0001t0008g0126 a0001c0001t0042g0223 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-26226A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108169056 | |||||||
chr12:108169500 | G | A | 5 | a0001c0001t0007g0026 a0001c0001t0024g0025 a0001c0001t0024g0030 others(2): Show |
5 | HG00438.hp1 NA18612.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.-551-25782G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108169500 | |||||||
chr12:108169880 | T | TA | 4 | a0001c0003t0022g0236 a0001c0003t0022g0257 a0001c0003t0031g0054 others(1): Show |
4 | HG01243.hp2 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-25400dupA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108169880 | ||||||
chr12:108169908 | C | G | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-25374C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108169908 | |||||||
chr12:108169909 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-551-25373G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108169909 | |||||||
chr12:108170036 | C | T | 1 | a0001c0001t0018g0031 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-551-25246C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170036 | |||||||
chr12:108170171 | GA | G | 148 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(145): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-551-25109delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108170171 | ||||||
chr12:108170173 | A | T | 148 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(145): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-551-25109A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170173 | |||||||
chr12:108170174 | C | A | 1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-551-25108C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170174 | |||||||
chr12:108170376 | A | AATG | 5 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0011g0092 others(2): Show |
5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-551-24896_-551-24 others(9): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108170376 | ||||||
chr12:108170445 | A | AATG | 3 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 |
3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-551-24817_-551-24 others(9): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108170445 | ||||||
chr12:108170468 | G | T | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-24814G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170468 | |||||||
chr12:108170586 | T | C | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-24696T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170586 | |||||||
chr12:108170703 | G | A | 2 | a0001c0001t0016g0269 a0002c0002t0010g0129 |
2 | HG00558.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-551-24579G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170703 | |||||||
chr12:108170793 | A | G | 1 | a0001c0001t0005g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-551-24489A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170793 | |||||||
chr12:108171025 | G | A | 1 | a0002c0002t0019g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-551-24257G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171025 | |||||||
chr12:108171119 | G | A | 5 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0011g0092 others(2): Show |
5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-551-24163G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171119 | |||||||
chr12:108171267 | G | C | 212 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(209): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-551-24015G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171267 | |||||||
chr12:108171300 | G | A | 28 | a0001c0001t0003g0006 a0001c0001t0003g0066 a0001c0001t0003g0067 others(25): Show |
30 | HG01081.hp1 HG01175.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-551-23982G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171300 | |||||||
chr12:108171335 | CA | C | 200 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(197): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.-551-23945delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108171335 | ||||||
chr12:108171383 | A | T | 1 | a0002c0002t0002g0215 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-551-23899A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171383 | |||||||
chr12:108171447 | T | A | 5 | a0001c0001t0023g0146 a0001c0001t0027g0013 a0001c0001t0059g0268 others(2): Show |
6 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-551-23835T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171447 | |||||||
chr12:108171512 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-551-23770C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171512 | |||||||
chr12:108171841 | A | G | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-23441A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171841 | |||||||
chr12:108171963 | A | G | 170 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(167): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-551-23319A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171963 | |||||||
chr12:108172010 | C | A | 2 | a0001c0001t0004g0114 a0001c0010t0046g0230 |
2 | HG01981.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-551-23272C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172010 | |||||||
chr12:108172073 | G | T | 8 | a0001c0001t0006g0088 a0001c0001t0007g0053 a0001c0001t0008g0126 others(5): Show |
8 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-23209G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172073 | |||||||
chr12:108172238 | G | A | 3 | a0001c0001t0015g0228 a0001c0001t0029g0226 a0001c0001t0029g0227 |
3 | HG01099.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-551-23044G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172238 | |||||||
chr12:108172405 | T | C | 1 | a0002c0002t0002g0262 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-551-22877T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172405 | |||||||
chr12:108172476 | T | C | 1 | a0002c0002t0001g0140 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-551-22806T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172476 | |||||||
chr12:108172601 | G | A | 167 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(164): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-551-22681G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172601 | |||||||
chr12:108172659 | C | T | 6 | a0001c0001t0016g0269 a0001c0001t0023g0146 a0001c0001t0027g0013 others(3): Show |
7 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-22623C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172659 | |||||||
chr12:108172746 | G | A | 11 | a0001c0001t0016g0269 a0001c0001t0023g0146 a0001c0001t0027g0013 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-551-22536G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172746 | |||||||
chr12:108173074 | C | T | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-22208C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173074 | |||||||
chr12:108173178 | C | A | 1 | a0002c0002t0001g0211 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-551-22104C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173178 | |||||||
chr12:108173419 | G | T | 156 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(153): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-551-21863G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173419 | |||||||
chr12:108173546 | A | G | 170 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(167): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-551-21736A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173546 | |||||||
chr12:108173606 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0019g0061 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-21676C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173606 | |||||||
chr12:108173607 | A | G | 208 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(205): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.-551-21675A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173607 | |||||||
chr12:108173716 | A | G | 1 | a0002c0002t0019g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-551-21566A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173716 | |||||||
chr12:108173804 | G | T | 1 | a0001c0001t0002g0192 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-551-21478G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173804 | |||||||
chr12:108173805 | G | GCT | 9 | a0001c0001t0002g0071 a0001c0001t0002g0079 a0001c0001t0002g0104 others(6): Show |
9 | HG00323.hp1 HG00597.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.-551-21472_-551-21 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173805 | ||||||
chr12:108173805 | G | GCTCT | 78 | a0001c0001t0001g0075 a0001c0001t0001g0081 a0001c0001t0001g0107 others(75): Show |
83 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-551-21474_-551-21 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173805 | ||||||
chr12:108173810 | C | CTCTCTCT others(11): Show |
1 | a0001c0001t0027g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(24): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTCTCTG | 39 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0084 others(36): Show |
39 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTCTCTGT others(1): Show |
17 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0143 others(14): Show |
18 | HG00735.hp1 HG01074.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTCTCTGT others(3): Show |
5 | a0001c0001t0003g0130 a0001c0001t0019g0062 a0002c0002t0003g0180 others(2): Show |
5 | HG00423.hp1 HG00558.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTCTCTGT others(7): Show |
2 | a0001c0001t0019g0061 a0006c0006t0016g0050 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(20): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTCTCTGT others(9): Show |
1 | a0001c0001t0023g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-551-21471_-551-21 others(22): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTCTCTGT others(11): Show |
1 | a0001c0001t0060g0267 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-551-21471_-551-21 others(24): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTCTCTGT others(13): Show |
2 | a0001c0001t0059g0268 a0001c0001t0061g0266 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(26): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTCTGTG | 3 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0057g0251 |
3 | HG01943.hp2 HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTCTGTGT others(1): Show |
3 | a0001c0001t0009g0052 a0001c0001t0035g0252 a0002c0002t0002g0261 |
3 | HG01099.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTG | 16 | a0001c0001t0004g0110 a0001c0001t0004g0120 a0001c0001t0004g0173 others(13): Show |
16 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-551-21428_-551-21 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTGTG | 8 | a0001c0001t0004g0109 a0001c0001t0005g0072 a0001c0001t0006g0007 others(5): Show |
9 | HG02280.hp2 HG03139.hp1 HG06807.hp1 others(6): Show |
intron_variant | MODIFIER | c.-551-21430_-551-21 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTGTGTG | 7 | a0001c0001t0004g0163 a0001c0001t0028g0231 a0001c0001t0036g0101 others(4): Show |
7 | HG00099.hp1 HG01981.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-21432_-551-21 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTGTGTGT others(1): Show |
4 | a0001c0001t0007g0053 a0001c0001t0016g0269 a0003c0004t0026g0058 others(1): Show |
4 | HG02723.hp1 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-21434_-551-21 others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTGTGTGT others(3): Show |
1 | a0001c0003t0012g0049 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-551-21436_-551-21 others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTGTGTGT others(5): Show |
5 | a0001c0001t0011g0060 a0001c0001t0015g0089 a0001c0001t0016g0048 others(2): Show |
5 | HG01243.hp2 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-21438_-551-21 others(18): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTGTGTGT others(7): Show |
6 | a0001c0001t0005g0090 a0001c0001t0011g0092 a0001c0001t0049g0128 others(3): Show |
6 | HG00642.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-551-21440_-551-21 others(20): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTGTGTGT others(9): Show |
2 | a0001c0001t0015g0091 a0001c0001t0030g0127 |
2 | HG01516.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-551-21442_-551-21 others(22): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTGTGTGT others(11): Show |
1 | a0001c0001t0008g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-551-21444_-551-21 others(24): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTGTGTGT others(13): Show |
1 | a0001c0001t0006g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-551-21446_-551-21 others(26): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | CTGTGTGT others(19): Show |
1 | a0001c0001t0005g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-551-21452_-551-21 others(32): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | C | G | 1 | a0001c0001t0043g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-21472C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173810 | |||||||
chr12:108173810 | CTG | C | 16 | a0001c0001t0003g0006 a0001c0001t0003g0066 a0001c0001t0003g0067 others(13): Show |
18 | HG01081.hp1 HG01109.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.-551-21428_-551-21 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173810 | CTGTG | C | 4 | a0001c0001t0004g0112 a0001c0001t0004g0114 a0001c0001t0016g0047 others(1): Show |
4 | HG01981.hp2 HG02257.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-21430_-551-21 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | ||||||
chr12:108173812 | G | C | 19 | a0001c0001t0001g0243 a0001c0001t0002g0071 a0001c0001t0002g0079 others(16): Show |
19 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.-551-21470G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173812 | |||||||
chr12:108173814 | G | C | 3 | a0001c0001t0002g0174 a0001c0001t0017g0212 a0001c0001t0062g0074 |
3 | HG02738.hp1 HG02970.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-551-21468G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173814 | |||||||
chr12:108174007 | C | T | 4 | a0001c0001t0023g0146 a0001c0001t0059g0268 a0001c0001t0060g0267 others(1): Show |
4 | HG01109.hp1 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-21275C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174007 | |||||||
chr12:108174105 | C | T | 1 | a0001c0001t0007g0034 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-551-21177C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174105 | |||||||
chr12:108174245 | A | G | 171 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(168): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-551-21037A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174245 | |||||||
chr12:108174260 | G | A | 1 | a0002c0002t0001g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-551-21022G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174260 | |||||||
chr12:108174474 | A | G | 1 | a0003c0004t0018g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-551-20808A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174474 | |||||||
chr12:108174662 | T | C | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-20620T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174662 | |||||||
chr12:108174691 | T | C | 4 | a0001c0003t0022g0236 a0001c0003t0022g0257 a0001c0003t0031g0054 others(1): Show |
4 | HG01243.hp2 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-20591T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174691 | |||||||
chr12:108174791 | G | A | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-20491G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174791 | |||||||
chr12:108174875 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0004g0112 others(1): Show |
5 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-20407G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174875 | |||||||
chr12:108174908 | G | C | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-20374G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174908 | |||||||
chr12:108174962 | G | A | 3 | a0001c0001t0019g0061 a0001c0001t0019g0062 a0006c0006t0016g0050 |
3 | HG02647.hp1 HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-551-20320G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174962 | |||||||
chr12:108175001 | G | A | 1 | a0001c0001t0018g0031 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-551-20281G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175001 | |||||||
chr12:108175055 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-551-20227C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175055 | |||||||
chr12:108175420 | T | C | 7 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0011g0092 others(4): Show |
7 | HG00642.hp2 HG01516.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-19862T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175420 | |||||||
chr12:108175449 | T | C | 4 | a0001c0001t0005g0001 a0001c0001t0005g0118 a0001c0001t0006g0001 others(1): Show |
5 | NA18941.hp1 NA18946.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-19833T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175449 | |||||||
chr12:108175455 | C | A | 14 | a0001c0001t0003g0006 a0001c0001t0003g0066 a0001c0001t0003g0067 others(11): Show |
16 | HG01081.hp1 HG01175.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-551-19827C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175455 | |||||||
chr12:108175527 | C | T | 149 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(146): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-551-19755C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175527 | |||||||
chr12:108175631 | T | C | 2 | a0001c0001t0015g0151 a0001c0001t0023g0150 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-551-19651T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175631 | |||||||
chr12:108175643 | C | T | 1 | a0001c0001t0053g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-551-19639C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175643 | |||||||
chr12:108175678 | T | C | 1 | a0002c0002t0010g0182 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-551-19604T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175678 | |||||||
chr12:108175692 | A | C | 5 | a0001c0003t0016g0059 a0001c0003t0022g0236 a0001c0003t0022g0257 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-19590A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175692 | |||||||
chr12:108175870 | C | T | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-19412C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175870 | |||||||
chr12:108175925 | C | T | 1 | a0002c0002t0001g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-551-19357C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175925 | |||||||
chr12:108175980 | C | T | 1 | a0002c0002t0001g0183 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-551-19302C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175980 | |||||||
chr12:108176121 | G | A | 21 | a0001c0001t0003g0006 a0001c0001t0003g0066 a0001c0001t0003g0067 others(18): Show |
23 | HG01081.hp1 HG01175.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-551-19161G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176121 | |||||||
chr12:108176134 | C | T | 9 | a0001c0001t0007g0019 a0001c0001t0007g0020 a0001c0001t0007g0029 others(6): Show |
9 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-551-19148C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176134 | |||||||
chr12:108176234 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-551-19048T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176234 | |||||||
chr12:108176247 | A | G | 187 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(184): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.-551-19035A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176247 | |||||||
chr12:108176325 | T | G | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-18957T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176325 | |||||||
chr12:108176508 | A | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0084 others(1): Show |
4 | HG00733.hp1 HG00735.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-18774A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176508 | |||||||
chr12:108176814 | GT | G | 164 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(161): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-551-18459delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108176814 | ||||||
chr12:108176895 | C | T | 2 | a0001c0001t0019g0061 a0001c0001t0019g0062 |
2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-551-18387C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176895 | |||||||
chr12:108177037 | A | G | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-551-18245A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177037 | |||||||
chr12:108177379 | C | T | 21 | a0001c0001t0003g0006 a0001c0001t0003g0066 a0001c0001t0003g0067 others(18): Show |
23 | HG01081.hp1 HG01175.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-551-17903C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177379 | |||||||
chr12:108177448 | C | G | 1 | a0001c0001t0020g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-551-17834C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177448 | |||||||
chr12:108177660 | C | T | 1 | a0001c0001t0016g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-551-17622C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177660 | |||||||
chr12:108177791 | C | T | 1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-551-17491C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177791 | |||||||
chr12:108177807 | G | A | 1 | a0001c0001t0009g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-551-17475G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177807 | |||||||
chr12:108177944 | G | A | 3 | a0001c0001t0019g0061 a0001c0001t0019g0062 a0006c0006t0016g0050 |
3 | HG02647.hp1 HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-551-17338G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177944 | |||||||
chr12:108178126 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-551-17156T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178126 | |||||||
chr12:108178342 | C | A | 4 | a0001c0001t0005g0001 a0001c0001t0005g0118 a0001c0001t0006g0001 others(1): Show |
5 | NA18941.hp1 NA18946.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-16940C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178342 | |||||||
chr12:108178343 | C | A | 32 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0202 others(29): Show |
32 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-551-16939C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178343 | |||||||
chr12:108178375 | T | C | 3 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 |
3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-551-16907T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178375 | |||||||
chr12:108178393 | C | T | 1 | a0001c0001t0016g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-551-16889C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178393 | |||||||
chr12:108178423 | C | T | 1 | a0001c0001t0007g0020 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-551-16859C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178423 | |||||||
chr12:108178424 | G | A | 21 | a0001c0001t0003g0006 a0001c0001t0003g0066 a0001c0001t0003g0067 others(18): Show |
23 | HG01081.hp1 HG01175.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-551-16858G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178424 | |||||||
chr12:108178461 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-551-16821C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178461 | |||||||
chr12:108178577 | C | A | 3 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 |
3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-551-16705C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178577 | |||||||
chr12:108178577 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-551-16705C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178577 | |||||||
chr12:108178582 | A | G | 1 | a0002c0002t0001g0197 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-551-16700A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178582 | |||||||
chr12:108178739 | G | A | 212 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(209): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-551-16543G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178739 | |||||||
chr12:108178797 | C | G | 6 | a0001c0001t0006g0088 a0001c0001t0007g0053 a0001c0001t0008g0126 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-551-16485C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178797 | |||||||
chr12:108178868 | C | G | 1 | a0001c0003t0031g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-551-16414C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178868 | |||||||
chr12:108178869 | G | A | 1 | a0001c0001t0028g0167 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-551-16413G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178869 | |||||||
chr12:108178942 | C | T | 20 | a0001c0001t0003g0006 a0001c0001t0003g0066 a0001c0001t0003g0067 others(17): Show |
22 | HG01081.hp1 HG01175.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-551-16340C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178942 | |||||||
chr12:108179058 | C | A | 1 | a0002c0002t0001g0179 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-551-16224C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179058 | |||||||
chr12:108179219 | A | G | 1 | a0001c0001t0010g0102 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-551-16063A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179219 | |||||||
chr12:108179265 | G | C | 18 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0011g0092 others(15): Show |
18 | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-551-16017G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179265 | |||||||
chr12:108179266 | G | T | 18 | a0001c0001t0005g0090 a0001c0001t0005g0093 a0001c0001t0011g0092 others(15): Show |
18 | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-551-16016G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179266 | |||||||
chr12:108179284 | G | A | 2 | a0001c0001t0006g0170 a0001c0001t0006g0233 |
2 | NA19012.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-551-15998G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179284 | |||||||
chr12:108179453 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-551-15829G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179453 | |||||||
chr12:108179520 | C | T | 2 | a0001c0001t0007g0053 a0001c0003t0012g0049 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-551-15762C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179520 | |||||||
chr12:108179767 | A | G | 1 | a0001c0001t0048g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-551-15515A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179767 | |||||||
chr12:108179913 | G | A | 10 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG00733.hp1 HG01069.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-551-15369G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179913 | |||||||
chr12:108180050 | CA | C | 174 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(171): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-551-15215delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108180050 | ||||||
chr12:108180050 | CAA | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0245 others(6): Show |
10 | HG01168.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-551-15216_-551-15 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108180050 | ||||||
chr12:108180055 | A | C | 6 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(3): Show |
7 | HG02257.hp1 NA18522.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-15227A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108180055 | |||||||
chr12:108180501 | T | G | 11 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(8): Show |
11 | HG00733.hp1 HG01069.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.-551-14781T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108180501 | |||||||
chr12:108180624 | C | G | 5 | a0001c0003t0016g0059 a0001c0003t0022g0236 a0001c0003t0022g0257 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-14658C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108180624 | |||||||
chr12:108180672 | G | T | 2 | a0001c0001t0059g0268 a0001c0001t0060g0267 |
2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-551-14610G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108180672 | |||||||
chr12:108180829 | C | T | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-14453C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108180829 | |||||||
chr12:108181048 | G | T | 4 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 others(1): Show |
4 | HG02257.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-14234G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181048 | |||||||
chr12:108181122 | T | G | 7 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(4): Show |
7 | HG00639.hp1 HG01099.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-14160T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181122 | |||||||
chr12:108181196 | C | T | 1 | a0001c0001t0006g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-551-14086C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181196 | |||||||
chr12:108181230 | C | A | 1 | a0001c0001t0006g0234 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-551-14052C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181230 | |||||||
chr12:108181257 | G | A | 4 | a0001c0001t0006g0117 a0001c0001t0006g0160 a0001c0001t0006g0161 others(1): Show |
4 | HG00735.hp2 HG01361.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-14025G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181257 | |||||||
chr12:108181260 | G | A | 2 | a0001c0001t0004g0173 a0001c0001t0005g0255 |
2 | HG02080.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-551-14022G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181260 | |||||||
chr12:108181285 | C | T | 1 | a0001c0001t0061g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-551-13997C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181285 | |||||||
chr12:108181491 | A | G | 1 | a0002c0002t0003g0191 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-551-13791A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181491 | |||||||
chr12:108181786 | A | G | 195 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(192): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-551-13496A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181786 | |||||||
chr12:108181817 | C | T | 1 | a0001c0001t0021g0256 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-551-13465C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181817 | |||||||
chr12:108181834 | C | A | 2 | a0001c0001t0019g0061 a0001c0001t0019g0062 |
2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-551-13448C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181834 | |||||||
chr12:108181834 | C | G | 1 | a0006c0006t0016g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-551-13448C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181834 | |||||||
chr12:108182215 | A | C | 164 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(161): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-551-13067A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108182215 | |||||||
chr12:108182221 | A | G | 195 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(192): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-551-13061A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108182221 | |||||||
chr12:108182425 | C | T | 2 | a0002c0002t0001g0011 a0002c0002t0002g0011 |
2 | HG01358.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-551-12857C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108182425 | |||||||
chr12:108182784 | G | A | 184 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(181): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-12498G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108182784 | |||||||
chr12:108182839 | GT | G | 17 | a0001c0001t0011g0014 a0001c0001t0011g0122 a0001c0001t0011g0124 others(14): Show |
18 | HG01109.hp1 HG01243.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-551-12432delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108182839 | ||||||
chr12:108183013 | GGGTCCAC others(1): Show |
G | 184 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(181): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-12266_-551-12 others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108183013 | ||||||
chr12:108183046 | A | G | 195 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(192): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-551-12236A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183046 | |||||||
chr12:108183082 | C | A | 1 | a0007c0011t0004g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-551-12200C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183082 | |||||||
chr12:108183353 | A | G | 1 | a0001c0001t0025g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-551-11929A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183353 | |||||||
chr12:108183610 | A | G | 195 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(192): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-551-11672A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183610 | |||||||
chr12:108183628 | G | A | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-11654G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183628 | |||||||
chr12:108183640 | C | T | 1 | a0001c0003t0016g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-551-11642C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183640 | |||||||
chr12:108183649 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0019g0061 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-11633A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183649 | |||||||
chr12:108183651 | C | A | 11 | a0001c0001t0008g0229 a0001c0001t0008g0253 a0001c0001t0011g0060 others(8): Show |
11 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-551-11631C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183651 | |||||||
chr12:108183770 | C | T | 8 | a0001c0001t0011g0014 a0001c0001t0011g0122 a0001c0001t0011g0124 others(5): Show |
9 | HG02280.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-551-11512C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183770 | |||||||
chr12:108184146 | C | G | 195 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(192): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-551-11136C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184146 | |||||||
chr12:108184206 | A | G | 195 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(192): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-551-11076A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184206 | |||||||
chr12:108184246 | G | A | 4 | a0001c0001t0004g0155 a0001c0001t0023g0146 a0001c0001t0030g0157 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-11036G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184246 | |||||||
chr12:108184277 | G | C | 1 | a0001c0001t0015g0091 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-551-11005G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184277 | |||||||
chr12:108184386 | G | T | 8 | a0001c0001t0005g0093 a0001c0001t0006g0088 a0001c0001t0007g0053 others(5): Show |
8 | HG02630.hp1 HG02683.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-10896G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184386 | |||||||
chr12:108184453 | C | A | 8 | a0001c0001t0005g0093 a0001c0001t0006g0088 a0001c0001t0007g0053 others(5): Show |
8 | HG02630.hp1 HG02683.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-10829C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184453 | |||||||
chr12:108184476 | G | A | 1 | a0001c0001t0061g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-551-10806G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184476 | |||||||
chr12:108184491 | C | T | 9 | a0001c0001t0011g0014 a0001c0001t0011g0122 a0001c0001t0011g0124 others(6): Show |
10 | HG02280.hp1 HG02572.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-551-10791C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184491 | |||||||
chr12:108184729 | A | G | 1 | a0001c0001t0056g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-551-10553A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184729 | |||||||
chr12:108185111 | T | C | 199 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(196): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-551-10171T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108185111 | |||||||
chr12:108185406 | G | A | 1 | a0001c0001t0005g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-551-9876G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108185406 | |||||||
chr12:108185605 | G | A | 184 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(181): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-9677G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108185605 | |||||||
chr12:108185619 | C | T | 2 | a0001c0001t0008g0229 a0001c0001t0008g0253 |
2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-551-9663C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108185619 | |||||||
chr12:108185670 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-551-9612G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108185670 | |||||||
chr12:108185730 | T | C | 9 | a0001c0001t0011g0014 a0001c0001t0011g0122 a0001c0001t0011g0124 others(6): Show |
10 | HG02280.hp1 HG02572.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-551-9552T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108185730 | |||||||
chr12:108186017 | G | A | 1 | a0001c0001t0027g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-551-9265G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186017 | |||||||
chr12:108186041 | C | T | 1 | a0001c0001t0066g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-551-9241C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186041 | |||||||
chr12:108186312 | G | A | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-8970G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186312 | |||||||
chr12:108186347 | C | T | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-8935C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186347 | |||||||
chr12:108186413 | C | T | 184 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(181): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-8869C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186413 | |||||||
chr12:108186597 | C | T | 184 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(181): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-8685C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186597 | |||||||
chr12:108186598 | G | A | 1 | a0001c0001t0043g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-8684G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186598 | |||||||
chr12:108186843 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-551-8439G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186843 | |||||||
chr12:108186901 | C | T | 184 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(181): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-8381C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186901 | |||||||
chr12:108186949 | C | G | 11 | a0001c0001t0008g0229 a0001c0001t0008g0253 a0001c0001t0011g0060 others(8): Show |
11 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-551-8333C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186949 | |||||||
chr12:108187169 | G | A | 184 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(181): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-8113G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108187169 | |||||||
chr12:108187317 | T | A | 1 | a0001c0001t0018g0018 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-551-7965T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108187317 | |||||||
chr12:108187325 | C | A | 2 | a0001c0001t0004g0110 a0001c0001t0004g0112 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-551-7957C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108187325 | |||||||
chr12:108187618 | A | G | 164 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(161): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-551-7664A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108187618 | |||||||
chr12:108187636 | AGT | A | 3 | a0001c0001t0008g0229 a0001c0001t0008g0253 a0007c0011t0004g0099 |
3 | HG02280.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-551-7643_-551-764 others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108187636 | ||||||
chr12:108187827 | G | A | 1 | a0001c0001t0006g0170 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-551-7455G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108187827 | |||||||
chr12:108187922 | C | G | 184 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(181): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-7360C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108187922 | |||||||
chr12:108188025 | C | T | 1 | a0001c0001t0003g0239 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-551-7257C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188025 | |||||||
chr12:108188351 | G | A | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-6931G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188351 | |||||||
chr12:108188521 | G | A | 50 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(47): Show |
52 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-551-6761G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188521 | |||||||
chr12:108188629 | A | T | 3 | a0001c0001t0001g0243 a0001c0001t0003g0244 a0002c0002t0010g0214 |
3 | HG02080.hp1 NA19000.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-551-6653A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188629 | |||||||
chr12:108188840 | T | C | 20 | a0001c0001t0009g0052 a0001c0001t0011g0014 a0001c0001t0011g0122 others(17): Show |
21 | HG01243.hp2 HG01943.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-551-6442T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188840 | |||||||
chr12:108188910 | C | A | 2 | a0001c0001t0015g0151 a0001c0001t0023g0150 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-551-6372C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188910 | |||||||
chr12:108188922 | T | C | 1 | a0001c0001t0043g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-6360T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188922 | |||||||
chr12:108189039 | G | A | 1 | a0001c0001t0043g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-6243G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189039 | |||||||
chr12:108189141 | T | C | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-6141T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189141 | |||||||
chr12:108189233 | C | T | 1 | a0001c0001t0043g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-6049C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189233 | |||||||
chr12:108189239 | C | T | 8 | a0001c0001t0008g0229 a0001c0001t0008g0253 a0001c0001t0011g0060 others(5): Show |
8 | HG02257.hp2 HG02280.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-551-6043C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189239 | |||||||
chr12:108189240 | G | A | 164 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(161): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-551-6042G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189240 | |||||||
chr12:108189313 | G | A | 5 | a0001c0003t0016g0059 a0001c0003t0022g0236 a0001c0003t0022g0257 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-5969G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189313 | |||||||
chr12:108189367 | C | G | 1 | a0001c0001t0018g0018 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-551-5915C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189367 | |||||||
chr12:108189453 | T | C | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-5829T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189453 | |||||||
chr12:108189484 | G | C | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-5798G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189484 | |||||||
chr12:108189662 | G | T | 1 | a0001c0001t0020g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-551-5620G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189662 | |||||||
chr12:108189702 | G | T | 1 | a0001c0001t0043g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-5580G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189702 | |||||||
chr12:108189821 | A | G | 207 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(204): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.-551-5461A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189821 | |||||||
chr12:108189896 | AT | A | 10 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG00733.hp1 HG01069.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-551-5384delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108189896 | ||||||
chr12:108190098 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0019g0061 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-5184G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190098 | |||||||
chr12:108190184 | C | T | 1 | a0002c0002t0001g0179 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-551-5098C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190184 | |||||||
chr12:108190196 | G | A | 2 | a0001c0001t0059g0268 a0001c0001t0060g0267 |
2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-551-5086G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190196 | |||||||
chr12:108190290 | G | A | 164 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(161): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-551-4992G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190290 | |||||||
chr12:108190366 | T | G | 2 | a0001c0001t0059g0268 a0001c0001t0060g0267 |
2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-551-4916T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190366 | |||||||
chr12:108190527 | G | T | 1 | a0001c0001t0012g0033 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-551-4755G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190527 | |||||||
chr12:108190837 | G | A | 1 | a0002c0002t0001g0210 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-551-4445G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190837 | |||||||
chr12:108191013 | C | T | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-4269C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191013 | |||||||
chr12:108191104 | T | G | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-4178T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191104 | |||||||
chr12:108191111 | G | A | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-4171G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191111 | |||||||
chr12:108191242 | A | G | 7 | a0001c0001t0008g0229 a0001c0001t0008g0253 a0001c0001t0011g0060 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-4040A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191242 | |||||||
chr12:108191367 | G | A | 1 | a0001c0001t0043g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-3915G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191367 | |||||||
chr12:108191473 | G | A | 4 | a0001c0001t0018g0031 a0001c0001t0026g0039 a0001c0001t0033g0037 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-3809G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191473 | |||||||
chr12:108191525 | G | A | 1 | a0001c0001t0008g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-551-3757G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191525 | |||||||
chr12:108191573 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-551-3709G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191573 | |||||||
chr12:108191592 | T | G | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-3690T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191592 | |||||||
chr12:108191768 | G | A | 1 | a0001c0001t0048g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-551-3514G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191768 | |||||||
chr12:108191863 | C | T | 8 | a0001c0001t0005g0093 a0001c0001t0006g0088 a0001c0001t0007g0053 others(5): Show |
8 | HG02630.hp1 HG02683.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-3419C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191863 | |||||||
chr12:108191878 | C | T | 1 | a0001c0001t0050g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-551-3404C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191878 | |||||||
chr12:108192050 | A | G | 184 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(181): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-3232A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192050 | |||||||
chr12:108192119 | C | G | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-551-3163C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192119 | |||||||
chr12:108192155 | T | A | 2 | a0001c0001t0059g0268 a0001c0001t0060g0267 |
2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-551-3127T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192155 | |||||||
chr12:108192205 | A | G | 7 | a0001c0001t0008g0229 a0001c0001t0008g0253 a0001c0001t0011g0060 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-3077A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192205 | |||||||
chr12:108192272 | G | A | 157 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(154): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-551-3010G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192272 | |||||||
chr12:108192461 | C | T | 8 | a0001c0001t0005g0093 a0001c0001t0006g0088 a0001c0001t0007g0053 others(5): Show |
8 | HG02630.hp1 HG02683.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-2821C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192461 | |||||||
chr12:108192513 | C | T | 4 | a0001c0001t0004g0155 a0001c0001t0023g0146 a0001c0001t0030g0157 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-2769C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192513 | |||||||
chr12:108192529 | T | A | 15 | a0001c0001t0005g0090 a0001c0001t0007g0034 a0001c0001t0009g0003 others(12): Show |
17 | HG00099.hp2 HG00642.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.-551-2753T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192529 | |||||||
chr12:108192529 | T | G | 8 | a0001c0001t0003g0239 a0001c0001t0006g0165 a0001c0001t0017g0094 others(5): Show |
8 | HG00323.hp2 HG01109.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-2753T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192529 | |||||||
chr12:108192554 | T | C | 191 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(188): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.-551-2728T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192554 | |||||||
chr12:108192773 | A | G | 207 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(204): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.-551-2509A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192773 | |||||||
chr12:108193025 | T | C | 1 | a0001c0001t0017g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-551-2257T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193025 | |||||||
chr12:108193213 | C | T | 184 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(181): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-2069C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193213 | |||||||
chr12:108193229 | A | G | 7 | a0001c0001t0008g0229 a0001c0001t0008g0253 a0001c0001t0011g0060 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-2053A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193229 | |||||||
chr12:108193277 | C | T | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-2005C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193277 | |||||||
chr12:108193350 | G | T | 20 | a0001c0001t0009g0052 a0001c0001t0011g0014 a0001c0001t0011g0122 others(17): Show |
21 | HG01243.hp2 HG01943.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-551-1932G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193350 | |||||||
chr12:108193367 | T | G | 1 | a0001c0001t0010g0102 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-551-1915T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193367 | |||||||
chr12:108193389 | T | A | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-1893T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193389 | |||||||
chr12:108193452 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-551-1830A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193452 | |||||||
chr12:108193567 | T | C | 3 | a0001c0001t0026g0039 a0001c0001t0033g0037 a0001c0001t0033g0038 |
3 | HG02895.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-551-1715T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193567 | |||||||
chr12:108193596 | A | AATGG | 184 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(181): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.-551-1667_-551-166 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108193596 | ||||||
chr12:108193596 | A | AATGGATG others(1): Show |
8 | a0001c0001t0011g0014 a0001c0001t0011g0122 a0001c0001t0011g0124 others(5): Show |
9 | HG02280.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-551-1671_-551-166 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108193596 | ||||||
chr12:108193603 | GGATGGAT others(9): Show |
G | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-1664_-551-164 others(20): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108193603 | ||||||
chr12:108193737 | G | A | 1 | a0001c0003t0016g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-551-1545G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193737 | |||||||
chr12:108193863 | T | C | 1 | a0001c0003t0031g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-551-1419T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193863 | |||||||
chr12:108193887 | T | C | 1 | a0001c0001t0043g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-1395T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193887 | |||||||
chr12:108194135 | T | C | 1 | a0001c0001t0011g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-551-1147T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194135 | |||||||
chr12:108194318 | G | A | 1 | a0001c0001t0043g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-964G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194318 | |||||||
chr12:108194353 | A | G | 184 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(181): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-929A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194353 | |||||||
chr12:108194363 | G | A | 19 | a0001c0001t0001g0133 a0001c0001t0002g0193 a0001c0001t0002g0201 others(16): Show |
20 | HG00558.hp2 HG00597.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.-551-919G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194363 | |||||||
chr12:108194456 | C | T | 7 | a0001c0001t0008g0229 a0001c0001t0008g0253 a0001c0001t0011g0060 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-826C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194456 | |||||||
chr12:108194516 | A | G | 2 | a0002c0002t0001g0194 a0002c0002t0003g0198 |
2 | NA18959.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-551-766A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194516 | |||||||
chr12:108194534 | A | T | 192 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(189): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-551-748A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194534 | |||||||
chr12:108194629 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-551-653A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194629 | |||||||
chr12:108194651 | T | C | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-631T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194651 | |||||||
chr12:108194692 | T | C | 192 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(189): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-551-590T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194692 | |||||||
chr12:108194846 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0019g0061 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-436A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194846 | |||||||
chr12:108195060 | ATCCAG | A | 14 | a0001c0001t0001g0098 a0001c0001t0001g0186 a0001c0001t0002g0008 others(11): Show |
15 | HG00597.hp2 HG00639.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.-551-221_-551-217d others(7): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108195060 | |||||||
chr12:108195077 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-551-205C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108195077 | |||||||
chr12:108195150 | A | G | 200 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(197): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-551-132A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108195150 | |||||||
chr12:108196291 | A | G | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.382+77A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108196291 | |||||||
chr12:108196404 | G | A | 2 | a0001c0001t0008g0111 a0001c0001t0063g0069 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382+190G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108196404 | |||||||
chr12:108196418 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.382+204C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108196418 | |||||||
chr12:108196499 | T | G | 1 | a0003c0004t0068g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382+285T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108196499 | |||||||
chr12:108196892 | A | G | 20 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+678A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108196892 | |||||||
chr12:108196963 | G | C | 20 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+749G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108196963 | |||||||
chr12:108197107 | T | C | 20 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+893T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197107 | |||||||
chr12:108197108 | AAG | A | 20 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+896_382+897del others(2): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108197108 | ||||||
chr12:108197112 | T | A | 20 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+898T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197112 | |||||||
chr12:108197113 | T | C | 20 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+899T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197113 | |||||||
chr12:108197114 | A | C | 20 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+900A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197114 | |||||||
chr12:108197115 | A | C | 20 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+901A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197115 | |||||||
chr12:108197228 | A | G | 1 | a0002c0002t0001g0210 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.382+1014A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197228 | |||||||
chr12:108197356 | C | T | 5 | a0001c0003t0016g0059 a0001c0003t0022g0236 a0001c0003t0022g0257 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+1142C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197356 | |||||||
chr12:108197403 | AG | A | 163 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0107 others(160): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.382+1192delG | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108197403 | ||||||
chr12:108197541 | G | A | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+1327G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197541 | |||||||
chr12:108197572 | A | G | 4 | a0001c0001t0004g0155 a0001c0001t0023g0146 a0001c0001t0030g0157 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+1358A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197572 | |||||||
chr12:108197841 | C | T | 1 | a0001c0003t0016g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.382+1627C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197841 | |||||||
chr12:108197943 | G | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0143 others(61): Show |
68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.382+1729G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197943 | |||||||
chr12:108197994 | A | T | 156 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0107 others(153): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.382+1780A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197994 | |||||||
chr12:108198025 | C | T | 1 | a0001c0003t0031g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.382+1811C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108198025 | |||||||
chr12:108198167 | C | A | 7 | a0001c0001t0008g0086 a0001c0001t0008g0113 a0001c0001t0008g0154 others(4): Show |
7 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.382+1953C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108198167 | |||||||
chr12:108198167 | C | T | 40 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(37): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.382+1953C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108198167 | |||||||
chr12:108198656 | T | C | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+2442T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108198656 | |||||||
chr12:108198826 | C | T | 5 | a0001c0001t0006g0165 a0001c0001t0017g0094 a0001c0001t0017g0095 others(2): Show |
5 | HG00323.hp2 HG01109.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+2612C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108198826 | |||||||
chr12:108199013 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.382+2799C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199013 | |||||||
chr12:108199055 | G | A | 35 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(32): Show |
36 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.382+2841G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199055 | |||||||
chr12:108199212 | T | C | 2 | a0001c0001t0007g0053 a0001c0003t0012g0049 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.382+2998T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199212 | |||||||
chr12:108199233 | C | T | 1 | a0001c0001t0003g0130 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.382+3019C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199233 | |||||||
chr12:108199243 | A | AT | 21 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(18): Show |
22 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.382+3033dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108199243 | ||||||
chr12:108199271 | C | T | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+3057C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199271 | |||||||
chr12:108199420 | C | T | 1 | a0001c0001t0033g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.382+3206C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199420 | |||||||
chr12:108199604 | G | A | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+3390G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199604 | |||||||
chr12:108199680 | T | G | 1 | a0001c0001t0005g0090 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.382+3466T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199680 | |||||||
chr12:108200092 | T | A | 1 | a0001c0001t0004g0163 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.382+3878T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108200092 | |||||||
chr12:108200266 | T | A | 98 | a0001c0001t0001g0075 a0001c0001t0001g0133 a0001c0001t0001g0202 others(95): Show |
100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.382+4052T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108200266 | |||||||
chr12:108200267 | C | A | 98 | a0001c0001t0001g0075 a0001c0001t0001g0133 a0001c0001t0001g0202 others(95): Show |
100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.382+4053C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108200267 | |||||||
chr12:108200292 | G | C | 96 | a0001c0001t0001g0075 a0001c0001t0001g0133 a0001c0001t0001g0202 others(93): Show |
98 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.382+4078G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108200292 | |||||||
chr12:108200489 | T | TTTCA | 41 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(38): Show |
43 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.382+4291_382+4294d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108200489 | ||||||
chr12:108200505 | A | T | 2 | a0001c0001t0005g0115 a0001c0001t0005g0116 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.382+4291A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108200505 | |||||||
chr12:108200730 | GGGGACCC others(7): Show |
G | 2 | a0001c0001t0007g0053 a0001c0003t0012g0049 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.382+4526_382+4539d others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108200730 | ||||||
chr12:108200923 | GGGTGGTC others(4): Show |
G | 1 | a0001c0001t0003g0239 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.382+4712_382+4722d others(13): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108200923 | ||||||
chr12:108200959 | A | C | 1 | a0002c0002t0010g0214 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.382+4745A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108200959 | |||||||
chr12:108201264 | T | A | 16 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(13): Show |
17 | HG00423.hp2 HG00639.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.383-5025T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201264 | |||||||
chr12:108201338 | G | A | 1 | a0001c0001t0003g0239 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.383-4951G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201338 | |||||||
chr12:108201476 | T | C | 1 | a0001c0001t0030g0127 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.383-4813T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201476 | |||||||
chr12:108201519 | T | TG | 65 | a0001c0001t0001g0075 a0001c0001t0001g0202 a0001c0001t0001g0218 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.383-4764dupG | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108201519 | ||||||
chr12:108201602 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0067g0063 |
4 | HG01884.hp2 HG01891.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-4687C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201602 | |||||||
chr12:108201760 | T | C | 47 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(44): Show |
49 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.383-4529T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201760 | |||||||
chr12:108201783 | C | A | 14 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(11): Show |
14 | HG00733.hp1 HG01069.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.383-4506C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201783 | |||||||
chr12:108201806 | C | T | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-4483C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201806 | |||||||
chr12:108202011 | C | T | 3 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 |
3 | HG02257.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.383-4278C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202011 | |||||||
chr12:108202062 | C | A | 5 | a0001c0003t0016g0059 a0001c0003t0022g0236 a0001c0003t0022g0257 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-4227C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202062 | |||||||
chr12:108202103 | G | A | 1 | a0002c0002t0001g0211 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.383-4186G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202103 | |||||||
chr12:108202121 | C | T | 1 | a0002c0002t0001g0200 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.383-4168C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202121 | |||||||
chr12:108202136 | CACGCTAA others(11): Show |
C | 6 | a0001c0001t0007g0053 a0001c0003t0012g0049 a0003c0004t0018g0056 others(3): Show |
6 | HG02109.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.383-4152_383-4135d others(20): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202136 | |||||||
chr12:108202197 | C | G | 2 | a0001c0001t0015g0169 a0001c0001t0021g0159 |
2 | HG02735.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.383-4092C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202197 | |||||||
chr12:108202330 | T | C | 14 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(11): Show |
14 | HG00733.hp1 HG01069.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.383-3959T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202330 | |||||||
chr12:108202346 | A | G | 98 | a0001c0001t0001g0075 a0001c0001t0001g0133 a0001c0001t0001g0202 others(95): Show |
100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.383-3943A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202346 | |||||||
chr12:108202531 | A | G | 109 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(106): Show |
111 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.383-3758A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202531 | |||||||
chr12:108202566 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0043g0147 others(6): Show |
10 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.383-3723T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202566 | |||||||
chr12:108202622 | C | T | 143 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(140): Show |
147 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.383-3667C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202622 | |||||||
chr12:108202726 | G | A | 1 | a0002c0002t0064g0205 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.383-3563G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202726 | |||||||
chr12:108202758 | G | A | 6 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(3): Show |
6 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.383-3531G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202758 | |||||||
chr12:108203038 | T | G | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-3251T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203038 | |||||||
chr12:108203111 | G | A | 16 | a0001c0001t0005g0090 a0001c0001t0007g0034 a0001c0001t0009g0003 others(13): Show |
17 | HG00642.hp2 HG01192.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.383-3178G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203111 | |||||||
chr12:108203137 | G | A | 2 | a0001c0001t0007g0053 a0001c0003t0012g0049 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.383-3152G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203137 | |||||||
chr12:108203177 | C | T | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-3112C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203177 | |||||||
chr12:108203294 | T | C | 1 | a0002c0002t0013g0188 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.383-2995T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203294 | |||||||
chr12:108203383 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.383-2906G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203383 | |||||||
chr12:108203463 | A | G | 4 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 others(1): Show |
4 | HG02257.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-2826A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203463 | |||||||
chr12:108203604 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0084 |
2 | HG00733.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.383-2685C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203604 | |||||||
chr12:108203623 | C | T | 2 | a0001c0001t0030g0127 a0001c0001t0049g0128 |
2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.383-2666C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203623 | |||||||
chr12:108203636 | C | T | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-2653C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203636 | |||||||
chr12:108203769 | T | C | 135 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(132): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.383-2520T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203769 | |||||||
chr12:108203881 | T | C | 6 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(3): Show |
6 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.383-2408T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203881 | |||||||
chr12:108204237 | T | A | 130 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(127): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.383-2052T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204237 | |||||||
chr12:108204259 | C | T | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-2030C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204259 | |||||||
chr12:108204359 | C | G | 1 | a0001c0001t0053g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.383-1930C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204359 | |||||||
chr12:108204384 | T | C | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.383-1905T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204384 | |||||||
chr12:108204496 | C | T | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1793C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204496 | |||||||
chr12:108204497 | G | A | 14 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(11): Show |
15 | HG00423.hp2 HG00639.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.383-1792G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204497 | |||||||
chr12:108204506 | A | C | 6 | a0001c0001t0001g0202 a0001c0001t0003g0138 a0001c0001t0007g0002 others(3): Show |
7 | HG00609.hp2 NA18944.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.383-1783A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204506 | |||||||
chr12:108204542 | G | A | 1 | a0001c0001t0005g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.383-1747G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204542 | |||||||
chr12:108204690 | T | G | 1 | a0002c0009t0001g0178 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.383-1599T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204690 | |||||||
chr12:108204764 | G | A | 1 | a0001c0001t0012g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.383-1525G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204764 | |||||||
chr12:108204822 | A | G | 2 | a0001c0001t0007g0053 a0001c0003t0012g0049 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.383-1467A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204822 | |||||||
chr12:108204910 | A | G | 213 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(210): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.383-1379A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204910 | |||||||
chr12:108204999 | C | CGA | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1290_383-1289i others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204999 | |||||||
chr12:108205018 | G | A | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1271G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205018 | |||||||
chr12:108205101 | C | T | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1188C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205101 | |||||||
chr12:108205159 | G | C | 13 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0011g0060 others(10): Show |
14 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.383-1130G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205159 | |||||||
chr12:108205178 | C | G | 1 | a0007c0011t0004g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.383-1111C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205178 | |||||||
chr12:108205226 | G | T | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.383-1063G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205226 | |||||||
chr12:108205252 | A | G | 1 | a0001c0001t0005g0171 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.383-1037A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205252 | |||||||
chr12:108205255 | T | A | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1034T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205255 | |||||||
chr12:108205287 | C | T | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1002C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205287 | |||||||
chr12:108205288 | G | A | 2 | a0002c0002t0003g0259 a0002c0002t0010g0129 |
2 | HG00558.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.383-1001G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205288 | |||||||
chr12:108205300 | C | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0043g0147 others(1): Show |
5 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-989C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205300 | |||||||
chr12:108205313 | C | T | 130 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(127): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.383-976C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205313 | |||||||
chr12:108205424 | T | C | 1 | a0001c0001t0004g0120 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.383-865T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205424 | |||||||
chr12:108205531 | G | GATTTATA | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-754_383-748dup others(7): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108205531 | ||||||
chr12:108205638 | T | C | 1 | a0007c0011t0004g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.383-651T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205638 | |||||||
chr12:108205864 | A | G | 2 | a0001c0001t0007g0053 a0001c0003t0012g0049 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.383-425A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205864 | |||||||
chr12:108205988 | T | C | 1 | a0001c0001t0003g0239 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.383-301T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205988 | |||||||
chr12:108205995 | C | T | 2 | a0001c0001t0059g0268 a0001c0001t0060g0267 |
2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.383-294C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205995 | |||||||
chr12:108206005 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.383-284G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108206005 | |||||||
chr12:108206035 | T | C | 1 | a0002c0002t0001g0200 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.383-254T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108206035 | |||||||
chr12:108206093 | A | G | 4 | a0001c0001t0004g0155 a0001c0001t0023g0146 a0001c0001t0030g0157 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-196A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108206093 | |||||||
chr12:108206416 | C | T | 1 | a0001c0003t0016g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497+13C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206416 | |||||||
chr12:108206460 | A | G | 130 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(127): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.497+57A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206460 | |||||||
chr12:108206511 | C | T | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.497+108C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206511 | |||||||
chr12:108206528 | T | C | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+125T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206528 | |||||||
chr12:108206657 | T | C | 1 | a0002c0002t0003g0191 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.497+254T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206657 | |||||||
chr12:108206698 | A | T | 13 | a0001c0001t0001g0133 a0001c0001t0002g0079 a0001c0001t0003g0260 others(10): Show |
14 | HG00597.hp2 HG01346.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+295A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206698 | |||||||
chr12:108206739 | C | A | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+336C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206739 | |||||||
chr12:108206783 | G | A | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+380G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206783 | |||||||
chr12:108207043 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0043g0147 others(1): Show |
5 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+640T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207043 | |||||||
chr12:108207086 | TA | T | 13 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0011g0060 others(10): Show |
14 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+684delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207086 | |||||||
chr12:108207339 | C | A | 126 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(123): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.497+936C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207339 | |||||||
chr12:108207351 | T | C | 1 | a0001c0001t0003g0260 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.497+948T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207351 | |||||||
chr12:108207388 | G | T | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.497+985G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207388 | |||||||
chr12:108207390 | G | C | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+987G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207390 | |||||||
chr12:108207533 | C | CT | 16 | a0001c0001t0001g0098 a0001c0001t0003g0006 a0001c0001t0004g0121 others(13): Show |
17 | HG00735.hp2 HG01175.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.497+1156dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 108207533 | ||||||
chr12:108207533 | C | CTTTT | 5 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0061g0266 others(2): Show |
6 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.497+1153_497+1156d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 108207533 | ||||||
chr12:108207533 | CT | C | 98 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(95): Show |
100 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.497+1156delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 108207533 | ||||||
chr12:108207533 | CTT | C | 21 | a0001c0001t0001g0084 a0001c0001t0001g0107 a0001c0001t0005g0093 others(18): Show |
22 | HG00099.hp2 HG00323.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.497+1155_497+1156d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 108207533 | ||||||
chr12:108207627 | T | C | 13 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0011g0060 others(10): Show |
14 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+1224T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207627 | |||||||
chr12:108207737 | G | A | 1 | a0003c0004t0018g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.497+1334G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207737 | |||||||
chr12:108207892 | T | A | 12 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0011g0060 others(9): Show |
13 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.497+1489T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207892 | |||||||
chr12:108207912 | G | T | 1 | a0001c0001t0011g0014 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.497+1509G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207912 | |||||||
chr12:108207939 | T | C | 31 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(28): Show |
32 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.497+1536T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207939 | |||||||
chr12:108207974 | G | A | 1 | a0001c0001t0004g0120 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.497+1571G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207974 | |||||||
chr12:108208026 | T | A | 13 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0011g0060 others(10): Show |
14 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+1623T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208026 | |||||||
chr12:108208110 | A | C | 124 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(121): Show |
127 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.497+1707A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208110 | |||||||
chr12:108208133 | G | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(121): Show |
127 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.497+1730G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208133 | |||||||
chr12:108208178 | G | C | 1 | a0001c0001t0003g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.497+1775G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208178 | |||||||
chr12:108208237 | TA | T | 4 | a0001c0001t0034g0250 a0001c0001t0035g0070 a0001c0001t0035g0252 others(1): Show |
4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+1836delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 108208237 | ||||||
chr12:108208269 | G | T | 6 | a0001c0001t0007g0026 a0001c0001t0024g0025 a0001c0001t0024g0030 others(3): Show |
6 | HG00438.hp1 NA18612.hp2 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-1852G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208269 | |||||||
chr12:108208378 | A | G | 6 | a0002c0002t0001g0140 a0002c0002t0001g0197 a0002c0002t0001g0200 others(3): Show |
6 | HG02015.hp2 HG02165.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-1743A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208378 | |||||||
chr12:108208468 | T | A | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-1653T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208468 | |||||||
chr12:108208538 | T | C | 1 | a0001c0003t0031g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.498-1583T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208538 | |||||||
chr12:108208634 | A | T | 126 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(123): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.498-1487A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208634 | |||||||
chr12:108208677 | G | C | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-1444G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208677 | |||||||
chr12:108208738 | G | C | 5 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(2): Show |
6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-1383G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208738 | |||||||
chr12:108208796 | T | C | 197 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(194): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.498-1325T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208796 | |||||||
chr12:108209078 | C | A | 3 | a0002c0002t0001g0145 a0002c0002t0001g0199 a0002c0002t0001g0210 |
3 | HG02145.hp1 HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.498-1043C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209078 | |||||||
chr12:108209078 | C | G | 102 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(99): Show |
104 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.498-1043C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209078 | |||||||
chr12:108209193 | C | A | 111 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(108): Show |
113 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.498-928C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209193 | |||||||
chr12:108209239 | A | G | 187 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(184): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.498-882A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209239 | |||||||
chr12:108209264 | T | C | 130 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(127): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.498-857T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209264 | |||||||
chr12:108209432 | G | A | 2 | a0001c0001t0008g0012 a0001c0001t0040g0012 |
2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.498-689G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209432 | |||||||
chr12:108209455 | T | C | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-666T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209455 | |||||||
chr12:108209583 | A | G | 13 | a0001c0001t0007g0053 a0001c0001t0011g0014 a0001c0001t0011g0122 others(10): Show |
14 | HG02280.hp1 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.498-538A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209583 | |||||||
chr12:108209640 | G | A | 3 | a0001c0001t0007g0053 a0001c0003t0012g0049 a0001c0003t0037g0065 |
3 | HG02647.hp2 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.498-481G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209640 | |||||||
chr12:108209752 | C | G | 20 | a0001c0001t0001g0107 a0001c0001t0004g0109 a0001c0001t0004g0110 others(17): Show |
21 | HG00099.hp2 HG01943.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.498-369C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209752 | |||||||
chr12:108209882 | T | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0245 others(35): Show |
41 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.498-239T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209882 | |||||||
chr12:108209922 | G | A | 2 | a0001c0001t0017g0212 a0001c0001t0017g0213 |
2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.498-199G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209922 | |||||||
chr12:108209949 | C | G | 1 | a0001c0001t0004g0163 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.498-172C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209949 | |||||||
chr12:108209991 | C | T | 1 | a0001c0001t0048g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.498-130C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209991 | |||||||
chr12:108210411 | C | T | 1 | a0006c0006t0016g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.682+106C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210411 | |||||||
chr12:108210445 | A | G | 32 | a0001c0001t0001g0107 a0001c0001t0004g0155 a0001c0001t0005g0093 others(29): Show |
33 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.682+140A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210445 | |||||||
chr12:108210455 | C | G | 196 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(193): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.682+150C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210455 | |||||||
chr12:108210603 | G | A | 1 | a0001c0001t0003g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.682+298G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210603 | |||||||
chr12:108210652 | T | C | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.682+347T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210652 | |||||||
chr12:108210799 | T | C | 33 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0006g0088 others(30): Show |
34 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.682+494T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210799 | |||||||
chr12:108210830 | G | A | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+525G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210830 | |||||||
chr12:108210931 | C | T | 1 | a0001c0001t0007g0034 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.682+626C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210931 | |||||||
chr12:108211145 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.682+840C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211145 | |||||||
chr12:108211250 | G | A | 2 | a0001c0001t0008g0111 a0001c0001t0063g0069 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.682+945G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211250 | |||||||
chr12:108211296 | T | C | 1 | a0001c0003t0012g0049 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.682+991T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211296 | |||||||
chr12:108211296 | T | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0043g0147 others(1): Show |
5 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+991T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211296 | |||||||
chr12:108211383 | A | G | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.682+1078A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211383 | |||||||
chr12:108211435 | C | T | 8 | a0001c0001t0007g0053 a0001c0003t0012g0049 a0001c0003t0016g0059 others(5): Show |
8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+1130C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211435 | |||||||
chr12:108211441 | G | T | 1 | a0001c0001t0008g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.682+1136G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211441 | |||||||
chr12:108211442 | C | G | 1 | a0001c0001t0008g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.682+1137C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211442 | |||||||
chr12:108211450 | T | C | 33 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0006g0088 others(30): Show |
34 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.682+1145T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211450 | |||||||
chr12:108211575 | G | A | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+1270G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211575 | |||||||
chr12:108211630 | C | CAT | 7 | a0001c0001t0004g0121 a0001c0001t0005g0001 a0001c0001t0006g0001 others(4): Show |
8 | HG00738.hp2 HG02135.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+1345_682+1346d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | ||||||
chr12:108211630 | C | CATAT | 32 | a0001c0001t0001g0149 a0001c0001t0001g0202 a0001c0001t0003g0138 others(29): Show |
33 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.682+1343_682+1346d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | ||||||
chr12:108211630 | C | CATATAT | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0023g0146 |
3 | HG01074.hp2 HG01515.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.682+1341_682+1346d others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | ||||||
chr12:108211630 | C | CATATATA others(5): Show |
3 | a0003c0004t0026g0057 a0003c0004t0026g0058 a0003c0004t0068g0217 |
3 | HG02109.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.682+1335_682+1346d others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | ||||||
chr12:108211630 | C | CATATATA others(17): Show |
1 | a0001c0001t0016g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.682+1338_682+1361d others(26): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | ||||||
chr12:108211630 | C | CATATATA others(19): Show |
1 | a0001c0001t0016g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.682+1336_682+1361d others(28): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | ||||||
chr12:108211630 | C | CATATATA others(19): Show |
3 | a0001c0001t0006g0234 a0001c0001t0011g0060 a0001c0001t0052g0235 |
3 | HG02922.hp1 NA18952.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.682+1346_682+1347i others(28): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | ||||||
chr12:108211630 | C | CATATATA others(31): Show |
1 | a0003c0004t0018g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.682+1346_682+1347i others(40): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | ||||||
chr12:108211630 | CAT | C | 131 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(128): Show |
135 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.682+1345_682+1346d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | ||||||
chr12:108211633 | A | ATATATAT others(3): Show |
2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.682+1337_682+1338i others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211633 | ||||||
chr12:108211649 | A | G | 1 | a0002c0002t0003g0180 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.682+1344A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211649 | |||||||
chr12:108211650 | T | TATAC | 8 | a0001c0001t0007g0053 a0001c0003t0012g0049 a0001c0003t0016g0059 others(5): Show |
8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+1346_682+1347i others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211650 | ||||||
chr12:108211667 | T | A | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.682+1362T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211667 | |||||||
chr12:108211746 | C | T | 12 | a0001c0001t0007g0053 a0001c0003t0012g0049 a0001c0003t0016g0059 others(9): Show |
12 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.682+1441C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211746 | |||||||
chr12:108211794 | G | C | 46 | a0001c0001t0001g0098 a0001c0001t0001g0107 a0001c0001t0001g0176 others(43): Show |
48 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.682+1489G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211794 | |||||||
chr12:108211803 | G | A | 4 | a0001c0003t0022g0236 a0001c0003t0022g0257 a0001c0003t0031g0054 others(1): Show |
4 | HG01243.hp2 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+1498G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211803 | |||||||
chr12:108211820 | A | AT | 85 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0082 others(82): Show |
87 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.682+1531dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211820 | ||||||
chr12:108211820 | A | ATT | 11 | a0001c0001t0001g0081 a0001c0001t0002g0174 a0001c0001t0004g0109 others(8): Show |
11 | HG00735.hp1 HG01074.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.682+1530_682+1531d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211820 | ||||||
chr12:108211820 | AT | A | 88 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0143 others(85): Show |
93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.682+1531delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211820 | ||||||
chr12:108211837 | G | T | 1 | a0001c0001t0004g0173 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.682+1532G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211837 | |||||||
chr12:108211948 | C | T | 1 | a0001c0001t0006g0233 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.682+1643C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211948 | |||||||
chr12:108212106 | C | G | 6 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0030g0127 others(3): Show |
7 | HG00099.hp2 HG01257.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+1801C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212106 | |||||||
chr12:108212200 | T | C | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.682+1895T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212200 | |||||||
chr12:108212245 | G | A | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.682+1940G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212245 | |||||||
chr12:108212251 | A | T | 10 | a0001c0001t0011g0014 a0001c0001t0011g0122 a0001c0001t0011g0124 others(7): Show |
11 | HG02280.hp1 HG02572.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.682+1946A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212251 | |||||||
chr12:108212285 | A | G | 18 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0011g0060 others(15): Show |
19 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.682+1980A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212285 | |||||||
chr12:108212322 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.682+2017G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212322 | |||||||
chr12:108212564 | C | G | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+2259C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212564 | |||||||
chr12:108212579 | T | C | 19 | a0001c0001t0011g0014 a0001c0001t0011g0060 a0001c0001t0011g0122 others(16): Show |
20 | HG01109.hp1 HG01943.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.682+2274T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212579 | |||||||
chr12:108212584 | C | G | 11 | a0001c0001t0007g0019 a0001c0001t0007g0020 a0001c0001t0007g0029 others(8): Show |
11 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(8): Show |
intron_variant | MODIFIER | c.682+2279C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212584 | |||||||
chr12:108212590 | T | TTC | 3 | a0001c0001t0005g0115 a0001c0001t0005g0116 a0001c0008t0020g0220 |
3 | HG01168.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.682+2308_682+2309d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212590 | ||||||
chr12:108212590 | TTCTC | T | 10 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 others(7): Show |
10 | HG01109.hp1 HG01943.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.682+2306_682+2309d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212590 | ||||||
chr12:108212609 | TCTCTCA | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0219 a0001c0001t0001g0221 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+2306_682+2311d others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212609 | ||||||
chr12:108212611 | T | A | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.682+2306T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212611 | |||||||
chr12:108212611 | T | TCACACAC others(7): Show |
3 | a0001c0001t0007g0053 a0001c0003t0012g0049 a0001c0003t0037g0065 |
3 | HG02647.hp2 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.682+2307_682+2308i others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212611 | ||||||
chr12:108212613 | T | A | 6 | a0001c0001t0001g0107 a0001c0001t0006g0088 a0001c0001t0007g0053 others(3): Show |
6 | HG02647.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.682+2308T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212613 | |||||||
chr12:108212613 | T | TCA | 13 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0004g0109 others(10): Show |
15 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.682+2329_682+2330d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212613 | ||||||
chr12:108212613 | T | TCACA | 13 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(10): Show |
14 | HG00423.hp2 HG00639.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.682+2327_682+2330d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212613 | ||||||
chr12:108212613 | T | TCACACAC others(9): Show |
5 | a0001c0003t0016g0059 a0001c0003t0022g0236 a0001c0003t0022g0257 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+2316_682+2317i others(18): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212613 | ||||||
chr12:108212613 | T | TCTCA | 30 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(27): Show |
31 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.682+2309_682+2310i others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212613 | ||||||
chr12:108212613 | T | TCTCACA | 3 | a0001c0001t0009g0021 a0001c0001t0009g0022 a0001c0001t0067g0063 |
3 | HG00642.hp1 HG01516.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.682+2309_682+2310i others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212613 | ||||||
chr12:108212613 | TCA | T | 84 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(81): Show |
85 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.682+2329_682+2330d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212613 | ||||||
chr12:108212615 | A | T | 3 | a0001c0001t0004g0163 a0001c0001t0014g0148 a0001c0008t0020g0220 |
3 | HG00099.hp1 HG01168.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.682+2310A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212615 | |||||||
chr12:108212616 | C | CACACAG | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+2316_682+2317i others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212616 | ||||||
chr12:108212618 | C | CACAG | 9 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0030g0127 others(6): Show |
10 | HG00099.hp2 HG01257.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.682+2316_682+2317i others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212618 | ||||||
chr12:108212618 | C | G | 3 | a0001c0001t0006g0088 a0001c0001t0008g0126 a0001c0001t0067g0063 |
3 | HG02809.hp1 HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.682+2313C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212618 | |||||||
chr12:108212640 | G | GAC | 13 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(10): Show |
14 | HG00423.hp2 HG00639.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.682+2348_682+2349d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212640 | ||||||
chr12:108212728 | C | T | 5 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(2): Show |
6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+2423C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212728 | |||||||
chr12:108212730 | A | C | 29 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0006g0088 others(26): Show |
30 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.682+2425A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212730 | |||||||
chr12:108212949 | A | G | 2 | a0001c0001t0027g0013 a0001c0001t0036g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.682+2644A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212949 | |||||||
chr12:108212973 | T | C | 26 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0006g0088 others(23): Show |
27 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.682+2668T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212973 | |||||||
chr12:108213091 | T | C | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.682+2786T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213091 | |||||||
chr12:108213179 | C | G | 1 | a0002c0002t0001g0211 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.682+2874C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213179 | |||||||
chr12:108213272 | G | A | 1 | a0002c0002t0001g0200 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.682+2967G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213272 | |||||||
chr12:108213597 | A | C | 5 | a0001c0001t0001g0249 a0001c0001t0002g0008 a0001c0001t0002g0104 others(2): Show |
6 | HG00423.hp2 HG02015.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+3292A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213597 | |||||||
chr12:108213601 | G | T | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.682+3296G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213601 | |||||||
chr12:108213790 | T | C | 1 | a0001c0001t0016g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.682+3485T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213790 | |||||||
chr12:108213836 | T | C | 1 | a0001c0001t0023g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.682+3531T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213836 | |||||||
chr12:108213839 | C | A | 93 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(90): Show |
94 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.682+3534C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213839 | |||||||
chr12:108213955 | A | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(38): Show |
43 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.682+3650A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213955 | |||||||
chr12:108214799 | T | C | 1 | a0001c0001t0007g0029 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.682+4494T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108214799 | |||||||
chr12:108214916 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.682+4611A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108214916 | |||||||
chr12:108215124 | T | C | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.682+4819T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215124 | |||||||
chr12:108215191 | G | T | 1 | a0001c0001t0004g0121 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.682+4886G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215191 | |||||||
chr12:108215361 | G | A | 67 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0143 others(64): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.682+5056G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215361 | |||||||
chr12:108215409 | C | T | 67 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0143 others(64): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.682+5104C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215409 | |||||||
chr12:108215555 | C | A | 1 | a0002c0002t0001g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.682+5250C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215555 | |||||||
chr12:108215637 | T | C | 67 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0143 others(64): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.682+5332T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215637 | |||||||
chr12:108215697 | G | C | 21 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0011g0060 others(18): Show |
22 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.682+5392G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215697 | |||||||
chr12:108215857 | G | A | 65 | a0001c0001t0001g0075 a0001c0001t0001g0218 a0001c0001t0001g0219 others(62): Show |
65 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.682+5552G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215857 | |||||||
chr12:108215921 | T | A | 14 | a0001c0001t0005g0090 a0001c0001t0007g0034 a0001c0001t0009g0003 others(11): Show |
15 | HG00642.hp2 HG01192.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.682+5616T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215921 | |||||||
chr12:108216108 | A | G | 223 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(220): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.682+5803A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216108 | |||||||
chr12:108216474 | C | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0143 others(60): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.682+6169C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216474 | |||||||
chr12:108216587 | G | A | 155 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(152): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.682+6282G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216587 | |||||||
chr12:108216623 | G | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(38): Show |
43 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.682+6318G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216623 | |||||||
chr12:108216706 | C | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0043g0147 others(1): Show |
5 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+6401C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216706 | |||||||
chr12:108216725 | A | G | 157 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.682+6420A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216725 | |||||||
chr12:108216821 | G | A | 7 | a0001c0003t0012g0049 a0001c0003t0016g0059 a0001c0003t0022g0236 others(4): Show |
7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+6516G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216821 | |||||||
chr12:108216843 | A | T | 197 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(194): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.682+6538A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216843 | |||||||
chr12:108216849 | G | A | 5 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(2): Show |
6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+6544G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216849 | |||||||
chr12:108216872 | G | A | 88 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(85): Show |
89 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.682+6567G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216872 | |||||||
chr12:108216899 | T | C | 157 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.682+6594T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216899 | |||||||
chr12:108217554 | G | A | 7 | a0001c0003t0012g0049 a0001c0003t0016g0059 a0001c0003t0022g0236 others(4): Show |
7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-7185G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108217554 | |||||||
chr12:108217648 | C | T | 164 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(161): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.683-7091C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108217648 | |||||||
chr12:108217697 | T | C | 91 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(88): Show |
92 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.683-7042T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108217697 | |||||||
chr12:108217741 | G | T | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.683-6998G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108217741 | |||||||
chr12:108217762 | C | G | 1 | a0001c0001t0002g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.683-6977C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108217762 | |||||||
chr12:108217799 | C | T | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.683-6940C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108217799 | |||||||
chr12:108217936 | G | GCTGGATC others(8): Show |
157 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.683-6801_683-6800i others(17): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108217936 | ||||||
chr12:108218027 | G | C | 197 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(194): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.683-6712G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218027 | |||||||
chr12:108218225 | A | T | 3 | a0001c0003t0016g0059 a0001c0003t0031g0054 a0001c0003t0031g0055 |
3 | HG01243.hp2 HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.683-6514A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218225 | |||||||
chr12:108218231 | G | C | 1 | a0001c0001t0006g0117 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.683-6508G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218231 | |||||||
chr12:108218283 | A | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0043g0147 others(1): Show |
5 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-6456A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218283 | |||||||
chr12:108218459 | A | G | 198 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(195): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.683-6280A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218459 | |||||||
chr12:108218464 | T | A | 1 | a0002c0002t0003g0180 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.683-6275T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218464 | |||||||
chr12:108218524 | A | G | 158 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(155): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.683-6215A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218524 | |||||||
chr12:108218624 | C | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(39): Show |
44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.683-6115C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218624 | |||||||
chr12:108219031 | C | T | 1 | a0001c0008t0020g0220 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.683-5708C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219031 | |||||||
chr12:108219143 | C | A | 1 | a0001c0003t0012g0049 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.683-5596C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219143 | |||||||
chr12:108219199 | T | C | 5 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(2): Show |
6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-5540T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219199 | |||||||
chr12:108219331 | C | T | 1 | a0002c0002t0002g0261 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.683-5408C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219331 | |||||||
chr12:108219374 | G | A | 91 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(88): Show |
92 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.683-5365G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219374 | |||||||
chr12:108219398 | G | A | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.683-5341G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219398 | |||||||
chr12:108219418 | A | G | 171 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(168): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.683-5321A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219418 | |||||||
chr12:108219464 | C | T | 1 | a0001c0001t0050g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.683-5275C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219464 | |||||||
chr12:108219496 | T | C | 1 | a0001c0001t0009g0041 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.683-5243T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219496 | |||||||
chr12:108219631 | C | A | 1 | a0002c0002t0010g0237 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.683-5108C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219631 | |||||||
chr12:108219684 | G | T | 15 | a0001c0001t0001g0075 a0001c0001t0001g0218 a0001c0001t0001g0219 others(12): Show |
16 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-5055G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219684 | |||||||
chr12:108219685 | T | C | 15 | a0001c0001t0001g0075 a0001c0001t0001g0218 a0001c0001t0001g0219 others(12): Show |
16 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-5054T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219685 | |||||||
chr12:108219846 | G | C | 4 | a0001c0001t0003g0138 a0001c0001t0007g0002 a0001c0001t0007g0016 others(1): Show |
5 | NA18944.hp1 NA18952.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-4893G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219846 | |||||||
chr12:108219991 | TG | T | 11 | a0001c0001t0001g0133 a0001c0001t0002g0079 a0001c0001t0004g0114 others(8): Show |
12 | HG00597.hp2 HG01346.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.683-4747delG | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219991 | |||||||
chr12:108220023 | C | T | 157 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.683-4716C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220023 | |||||||
chr12:108220052 | C | G | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-4687C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220052 | |||||||
chr12:108220126 | T | A | 156 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(153): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.683-4613T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220126 | |||||||
chr12:108220184 | CA | C | 4 | a0001c0003t0012g0049 a0001c0003t0022g0236 a0001c0003t0022g0257 others(1): Show |
4 | HG02615.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-4553delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108220184 | ||||||
chr12:108220269 | T | C | 158 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(155): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.683-4470T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220269 | |||||||
chr12:108220287 | C | T | 157 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.683-4452C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220287 | |||||||
chr12:108220538 | G | A | 65 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0143 others(62): Show |
68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.683-4201G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220538 | |||||||
chr12:108220563 | T | G | 7 | a0001c0003t0012g0049 a0001c0003t0016g0059 a0001c0003t0022g0236 others(4): Show |
7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-4176T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220563 | |||||||
chr12:108220704 | T | A | 7 | a0001c0003t0012g0049 a0001c0003t0016g0059 a0001c0003t0022g0236 others(4): Show |
7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-4035T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220704 | |||||||
chr12:108220836 | C | A | 1 | a0001c0001t0011g0122 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.683-3903C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220836 | |||||||
chr12:108220951 | C | T | 6 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0030g0127 others(3): Show |
7 | HG00099.hp2 HG01257.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-3788C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220951 | |||||||
chr12:108220971 | T | G | 158 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(155): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.683-3768T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220971 | |||||||
chr12:108221058 | T | A | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.683-3681T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221058 | |||||||
chr12:108221123 | A | G | 1 | a0001c0001t0042g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.683-3616A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221123 | |||||||
chr12:108221176 | G | A | 1 | a0001c0001t0003g0103 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.683-3563G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221176 | |||||||
chr12:108221180 | G | A | 157 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.683-3559G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221180 | |||||||
chr12:108221293 | G | A | 7 | a0001c0003t0012g0049 a0001c0003t0016g0059 a0001c0003t0022g0236 others(4): Show |
7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-3446G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221293 | |||||||
chr12:108221571 | C | T | 1 | a0001c0001t0016g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.683-3168C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221571 | |||||||
chr12:108221678 | C | T | 2 | a0001c0003t0012g0049 a0001c0003t0037g0065 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.683-3061C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221678 | |||||||
chr12:108221694 | A | G | 171 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(168): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.683-3045A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221694 | |||||||
chr12:108221695 | A | C | 171 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(168): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.683-3044A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221695 | |||||||
chr12:108221789 | G | A | 2 | a0001c0001t0027g0013 a0001c0001t0036g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.683-2950G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221789 | |||||||
chr12:108221848 | C | A | 1 | a0001c0003t0016g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.683-2891C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221848 | |||||||
chr12:108222058 | A | G | 2 | a0002c0002t0001g0011 a0002c0002t0002g0011 |
2 | HG01358.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.683-2681A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222058 | |||||||
chr12:108222157 | T | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.683-2582T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222157 | |||||||
chr12:108222320 | A | C | 1 | a0001c0001t0003g0244 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.683-2419A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222320 | |||||||
chr12:108222346 | G | A | 1 | a0001c0001t0042g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.683-2393G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222346 | |||||||
chr12:108222413 | G | A | 1 | a0001c0001t0004g0155 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.683-2326G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222413 | |||||||
chr12:108222487 | A | G | 1 | a0001c0001t0005g0072 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.683-2252A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222487 | |||||||
chr12:108222709 | G | T | 1 | a0001c0001t0011g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.683-2030G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222709 | |||||||
chr12:108222717 | C | T | 7 | a0001c0001t0003g0258 a0001c0001t0005g0072 a0001c0001t0005g0171 others(4): Show |
8 | NA18940.hp1 NA18940.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.683-2022C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222717 | |||||||
chr12:108222724 | C | T | 1 | a0001c0001t0005g0158 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.683-2015C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222724 | |||||||
chr12:108222767 | A | G | 170 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(167): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.683-1972A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222767 | |||||||
chr12:108222845 | T | C | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.683-1894T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222845 | |||||||
chr12:108222875 | G | C | 1 | a0001c0001t0034g0224 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.683-1864G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222875 | |||||||
chr12:108222905 | T | C | 2 | a0001c0001t0030g0127 a0001c0001t0049g0128 |
2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.683-1834T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222905 | |||||||
chr12:108222958 | G | A | 1 | a0001c0001t0002g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.683-1781G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222958 | |||||||
chr12:108222982 | G | A | 1 | a0001c0001t0017g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.683-1757G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222982 | |||||||
chr12:108222992 | T | C | 2 | a0002c0002t0001g0183 a0002c0002t0002g0215 |
2 | HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.683-1747T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222992 | |||||||
chr12:108223120 | A | G | 4 | a0001c0003t0012g0049 a0001c0003t0022g0236 a0001c0003t0022g0257 others(1): Show |
4 | HG02615.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-1619A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108223120 | |||||||
chr12:108223608 | T | C | 171 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(168): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.683-1131T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108223608 | |||||||
chr12:108223934 | G | T | 1 | a0001c0001t0013g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.683-805G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108223934 | |||||||
chr12:108223978 | G | A | 1 | a0001c0001t0042g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.683-761G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108223978 | |||||||
chr12:108224237 | A | G | 67 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0143 others(64): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.683-502A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224237 | |||||||
chr12:108224240 | ACTTTTCC others(14): Show |
A | 67 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0143 others(64): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.683-497_683-477del others(21): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108224240 | ||||||
chr12:108224304 | C | T | 2 | a0001c0001t0005g0115 a0001c0001t0005g0116 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.683-435C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224304 | |||||||
chr12:108224321 | C | A | 1 | a0002c0002t0013g0187 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.683-418C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224321 | |||||||
chr12:108224454 | A | G | 4 | a0001c0001t0012g0033 a0001c0001t0012g0036 a0001c0001t0012g0044 others(1): Show |
4 | HG01943.hp1 HG02683.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-285A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224454 | |||||||
chr12:108224476 | A | G | 171 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(168): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.683-263A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224476 | |||||||
chr12:108224514 | G | A | 2 | a0002c0002t0001g0134 a0002c0002t0001g0175 |
2 | NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.683-225G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224514 | |||||||
chr12:108224555 | A | G | 1 | a0001c0001t0004g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.683-184A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224555 | |||||||
chr12:108224957 | C | T | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+97C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108224957 | |||||||
chr12:108224992 | G | A | 22 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0011g0060 others(19): Show |
23 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.804+132G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108224992 | |||||||
chr12:108225018 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.804+158G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225018 | |||||||
chr12:108225065 | A | G | 171 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(168): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.804+205A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225065 | |||||||
chr12:108225075 | G | GT | 171 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(168): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.804+218dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 108225075 | ||||||
chr12:108225285 | G | A | 171 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(168): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.804+425G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225285 | |||||||
chr12:108225566 | C | G | 170 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(167): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.804+706C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225566 | |||||||
chr12:108225586 | C | T | 7 | a0001c0003t0012g0049 a0001c0003t0016g0059 a0001c0003t0022g0236 others(4): Show |
7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.804+726C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225586 | |||||||
chr12:108225618 | T | TG | 171 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(168): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.804+760dupG | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 108225618 | ||||||
chr12:108225691 | C | G | 1 | a0001c0001t0013g0248 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.804+831C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225691 | |||||||
chr12:108225834 | G | T | 1 | a0001c0001t0003g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.804+974G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225834 | |||||||
chr12:108225910 | C | A | 5 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(2): Show |
6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+1050C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225910 | |||||||
chr12:108225920 | G | C | 32 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(29): Show |
33 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.804+1060G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225920 | |||||||
chr12:108226040 | C | A | 22 | a0001c0001t0001g0107 a0001c0001t0005g0093 a0001c0001t0011g0060 others(19): Show |
23 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.805-950C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226040 | |||||||
chr12:108226244 | G | A | 65 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0143 others(62): Show |
68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.805-746G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226244 | |||||||
chr12:108226265 | C | T | 12 | a0001c0001t0001g0133 a0001c0001t0002g0079 a0001c0001t0004g0114 others(9): Show |
13 | HG00597.hp2 HG01346.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.805-725C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226265 | |||||||
chr12:108226333 | G | C | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.805-657G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226333 | |||||||
chr12:108226469 | G | T | 11 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 others(8): Show |
11 | HG01109.hp1 HG01943.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.805-521G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226469 | |||||||
chr12:108226625 | T | C | 67 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0143 others(64): Show |
70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.805-365T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226625 | |||||||
chr12:108226797 | T | C | 2 | a0001c0001t0004g0121 a0001c0001t0017g0096 |
2 | HG01433.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.805-193T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226797 | |||||||
chr12:108226913 | C | A | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.805-77C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226913 | |||||||
chr12:108227480 | G | A | 7 | a0001c0003t0012g0049 a0001c0003t0016g0059 a0001c0003t0022g0236 others(4): Show |
7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+316G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227480 | |||||||
chr12:108227533 | C | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(39): Show |
44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.979+369C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227533 | |||||||
chr12:108227641 | A | C | 171 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(168): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.979+477A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227641 | |||||||
chr12:108227660 | C | A | 1 | a0001c0001t0065g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.979+496C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227660 | |||||||
chr12:108227660 | C | T | 1 | a0001c0001t0042g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.979+496C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227660 | |||||||
chr12:108227700 | G | C | 1 | a0001c0001t0042g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.979+536G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227700 | |||||||
chr12:108227727 | G | GTGA | 93 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(90): Show |
94 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.979+587_979+589dup others(3): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 108227727 | ||||||
chr12:108227727 | G | GTGATAA | 3 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 |
3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.979+567_979+568ins others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 108227727 | ||||||
chr12:108227727 | G | GTGATGA | 72 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0107 others(69): Show |
76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.979+584_979+589dup others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 108227727 | ||||||
chr12:108227727 | G | GTGATGAT others(8): Show |
2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.979+575_979+589dup others(15): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 108227727 | ||||||
chr12:108227845 | C | T | 5 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(2): Show |
6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.979+681C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227845 | |||||||
chr12:108227887 | C | T | 170 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(167): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.979+723C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227887 | |||||||
chr12:108228103 | G | A | 1 | a0001c0001t0041g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.979+939G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228103 | |||||||
chr12:108228134 | C | A | 4 | a0001c0003t0012g0049 a0001c0003t0022g0236 a0001c0003t0022g0257 others(1): Show |
4 | HG02615.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+970C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228134 | |||||||
chr12:108228147 | A | T | 1 | a0001c0008t0020g0220 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.979+983A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228147 | |||||||
chr12:108228165 | G | C | 170 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(167): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.979+1001G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228165 | |||||||
chr12:108228181 | T | A | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0013g0204 others(3): Show |
6 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.979+1017T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228181 | |||||||
chr12:108228295 | C | T | 5 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(2): Show |
5 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.979+1131C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228295 | |||||||
chr12:108228315 | T | A | 171 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(168): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.979+1151T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228315 | |||||||
chr12:108228358 | C | T | 1 | a0001c0001t0048g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.979+1194C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228358 | |||||||
chr12:108228415 | T | C | 1 | a0002c0002t0001g0175 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.979+1251T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228415 | |||||||
chr12:108228565 | T | C | 1 | a0007c0011t0004g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.979+1401T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228565 | |||||||
chr12:108228725 | G | A | 1 | a0002c0002t0003g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.979+1561G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228725 | |||||||
chr12:108228907 | G | T | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.979+1743G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228907 | |||||||
chr12:108228956 | A | C | 2 | a0001c0001t0030g0127 a0001c0001t0049g0128 |
2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.979+1792A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228956 | |||||||
chr12:108229050 | T | A | 9 | a0001c0001t0006g0088 a0001c0001t0008g0126 a0001c0003t0012g0049 others(6): Show |
9 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.979+1886T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229050 | |||||||
chr12:108229076 | C | A | 2 | a0002c0002t0001g0134 a0002c0002t0001g0175 |
2 | NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.979+1912C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229076 | |||||||
chr12:108229106 | G | T | 192 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(189): Show |
198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.979+1942G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229106 | |||||||
chr12:108229111 | G | A | 1 | a0001c0001t0006g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.979+1947G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229111 | |||||||
chr12:108229265 | C | G | 2 | a0001c0001t0034g0250 a0001c0001t0057g0251 |
2 | HG01943.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.979+2101C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229265 | |||||||
chr12:108229724 | T | C | 1 | a0002c0002t0002g0181 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.979+2560T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229724 | |||||||
chr12:108229783 | T | G | 1 | a0001c0001t0007g0026 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.979+2619T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229783 | |||||||
chr12:108229790 | G | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0061g0266 |
4 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+2626G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229790 | |||||||
chr12:108229865 | G | GA | 16 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(13): Show |
17 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.979+2718dupA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 108229865 | ||||||
chr12:108229865 | GAA | G | 43 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(40): Show |
45 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.979+2717_979+2718d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 108229865 | ||||||
chr12:108229866 | A | G | 1 | a0001c0001t0011g0060 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.979+2702A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229866 | |||||||
chr12:108229903 | G | A | 1 | a0002c0002t0010g0214 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.979+2739G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229903 | |||||||
chr12:108229949 | T | C | 2 | a0001c0001t0008g0111 a0001c0001t0063g0069 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.980-2782T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229949 | |||||||
chr12:108229959 | A | G | 44 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(41): Show |
46 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.980-2772A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229959 | |||||||
chr12:108229976 | T | C | 42 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(39): Show |
44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.980-2755T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229976 | |||||||
chr12:108230030 | G | A | 1 | a0002c0002t0001g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.980-2701G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230030 | |||||||
chr12:108230249 | G | A | 213 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(210): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.980-2482G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230249 | |||||||
chr12:108230441 | C | T | 56 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(53): Show |
59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.980-2290C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230441 | |||||||
chr12:108230451 | C | G | 42 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(39): Show |
44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.980-2280C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230451 | |||||||
chr12:108230501 | G | A | 42 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(39): Show |
44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.980-2230G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230501 | |||||||
chr12:108230593 | G | A | 5 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(2): Show |
6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-2138G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230593 | |||||||
chr12:108230763 | G | A | 2 | a0001c0001t0004g0155 a0001c0001t0041g0156 |
2 | HG01891.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.980-1968G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230763 | |||||||
chr12:108230769 | T | C | 7 | a0001c0003t0012g0049 a0001c0003t0016g0059 a0001c0003t0022g0236 others(4): Show |
7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.980-1962T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230769 | |||||||
chr12:108230812 | C | T | 1 | a0001c0001t0054g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.980-1919C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230812 | |||||||
chr12:108230920 | C | G | 4 | a0003c0004t0018g0056 a0003c0004t0026g0057 a0003c0004t0026g0058 others(1): Show |
4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.980-1811C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230920 | |||||||
chr12:108230940 | T | C | 1 | a0001c0001t0004g0164 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.980-1791T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230940 | |||||||
chr12:108230952 | G | C | 2 | a0001c0001t0003g0066 a0001c0001t0036g0064 |
2 | HG01081.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.980-1779G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230952 | |||||||
chr12:108231255 | C | G | 2 | a0001c0001t0006g0088 a0001c0001t0008g0126 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.980-1476C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108231255 | |||||||
chr12:108231308 | C | T | 43 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(40): Show |
45 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.980-1423C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108231308 | |||||||
chr12:108231685 | G | A | 268 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(265): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.980-1046G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108231685 | |||||||
chr12:108231894 | C | G | 48 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(45): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.980-837C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108231894 | |||||||
chr12:108232196 | C | G | 1 | a0002c0002t0003g0198 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.980-535C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108232196 | |||||||
chr12:108232463 | C | A | 1 | a0001c0001t0062g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.980-268C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108232463 | |||||||
chr12:108232654 | G | A | 43 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(40): Show |
45 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.980-77G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108232654 | |||||||
chr12:108232694 | C | G | 12 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(9): Show |
13 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.980-37C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108232694 | |||||||
chr12:108232950 | C | T | 1 | a0001c0001t0018g0031 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1144+55C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108232950 | |||||||
chr12:108233047 | A | AC | 14 | a0001c0001t0002g0192 a0001c0001t0004g0109 a0001c0001t0004g0110 others(11): Show |
15 | HG01243.hp2 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1144+159dupC | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 108233047 | ||||||
chr12:108233052 | C | A | 43 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(40): Show |
45 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.1144+157C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233052 | |||||||
chr12:108233055 | A | C | 1 | a0001c0001t0042g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1144+160A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233055 | |||||||
chr12:108233055 | A | G | 12 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(9): Show |
13 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144+160A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233055 | |||||||
chr12:108233085 | A | G | 56 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(53): Show |
59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1144+190A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233085 | |||||||
chr12:108233292 | A | G | 1 | a0002c0002t0019g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1144+397A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233292 | |||||||
chr12:108233402 | C | T | 14 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(11): Show |
15 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1144+507C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233402 | |||||||
chr12:108233619 | A | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(42): Show |
47 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.1144+724A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233619 | |||||||
chr12:108233650 | A | AT | 42 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(39): Show |
44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.1144+765dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 108233650 | ||||||
chr12:108233672 | T | C | 3 | a0001c0003t0016g0059 a0001c0003t0031g0054 a0001c0003t0031g0055 |
3 | HG01243.hp2 HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1144+777T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233672 | |||||||
chr12:108233676 | G | A | 12 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(9): Show |
13 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144+781G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233676 | |||||||
chr12:108234011 | C | T | 13 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(10): Show |
14 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1144+1116C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234011 | |||||||
chr12:108234192 | G | A | 1 | a0002c0009t0001g0178 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1144+1297G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234192 | |||||||
chr12:108234217 | G | A | 2 | a0001c0001t0006g0170 a0001c0001t0006g0233 |
2 | NA19012.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1144+1322G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234217 | |||||||
chr12:108234272 | G | A | 1 | a0001c0001t0062g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1144+1377G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234272 | |||||||
chr12:108234290 | T | C | 91 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(88): Show |
92 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1144+1395T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234290 | |||||||
chr12:108234539 | C | T | 12 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(9): Show |
13 | HG00639.hp2 HG02015.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.1144+1644C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234539 | |||||||
chr12:108234842 | G | A | 2 | a0001c0001t0027g0013 a0001c0001t0036g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1144+1947G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234842 | |||||||
chr12:108234864 | A | G | 2 | a0001c0001t0030g0127 a0001c0001t0049g0128 |
2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1144+1969A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234864 | |||||||
chr12:108234955 | G | A | 2 | a0001c0001t0036g0064 a0002c0002t0001g0175 |
2 | HG02622.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1144+2060G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234955 | |||||||
chr12:108234977 | G | A | 1 | a0001c0001t0020g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1144+2082G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234977 | |||||||
chr12:108235019 | C | T | 12 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(9): Show |
13 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144+2124C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235019 | |||||||
chr12:108235199 | A | G | 1 | a0002c0002t0003g0180 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1144+2304A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235199 | |||||||
chr12:108235238 | T | C | 1 | a0001c0001t0042g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1144+2343T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235238 | |||||||
chr12:108235316 | G | A | 1 | a0001c0001t0036g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1144+2421G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235316 | |||||||
chr12:108235317 | G | A | 12 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(9): Show |
13 | HG00639.hp2 HG02015.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.1144+2422G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235317 | |||||||
chr12:108235325 | G | T | 13 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(10): Show |
14 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1144+2430G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235325 | |||||||
chr12:108235524 | C | G | 1 | a0002c0002t0001g0199 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1144+2629C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235524 | |||||||
chr12:108235792 | T | G | 1 | a0001c0001t0002g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1144+2897T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235792 | |||||||
chr12:108235874 | G | A | 1 | a0002c0002t0001g0211 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1144+2979G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235874 | |||||||
chr12:108235882 | A | G | 197 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(194): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1144+2987A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235882 | |||||||
chr12:108235965 | G | A | 1 | a0001c0003t0031g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1144+3070G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235965 | |||||||
chr12:108236003 | G | A | 49 | a0001c0001t0001g0243 a0001c0001t0001g0249 a0001c0001t0003g0244 others(46): Show |
49 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1144+3108G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236003 | |||||||
chr12:108236004 | C | A | 1 | a0001c0001t0042g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1144+3109C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236004 | |||||||
chr12:108236011 | C | T | 1 | a0001c0001t0008g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1144+3116C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236011 | |||||||
chr12:108236051 | G | A | 1 | a0001c0001t0042g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1144+3156G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236051 | |||||||
chr12:108236531 | C | T | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1144+3636C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236531 | |||||||
chr12:108236553 | C | T | 1 | a0001c0003t0016g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1144+3658C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236553 | |||||||
chr12:108236582 | TTC | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(50): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1144+3703_1144+370 others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 108236582 | ||||||
chr12:108236600 | A | C | 1 | a0007c0011t0004g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1144+3705A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236600 | |||||||
chr12:108236837 | C | T | 13 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0112 others(10): Show |
14 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1145-3507C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236837 | |||||||
chr12:108237066 | C | T | 1 | a0004c0007t0024g0028 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1145-3278C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237066 | |||||||
chr12:108237212 | C | T | 181 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(178): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1145-3132C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237212 | |||||||
chr12:108237270 | G | A | 141 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(138): Show |
145 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1145-3074G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237270 | |||||||
chr12:108237417 | G | T | 1 | a0001c0001t0023g0232 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1145-2927G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237417 | |||||||
chr12:108237439 | G | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(37): Show |
42 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1145-2905G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237439 | |||||||
chr12:108237505 | C | T | 16 | a0001c0001t0001g0075 a0001c0001t0001g0218 a0001c0001t0001g0219 others(13): Show |
17 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1145-2839C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237505 | |||||||
chr12:108237783 | C | G | 2 | a0001c0001t0015g0151 a0001c0001t0023g0150 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1145-2561C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237783 | |||||||
chr12:108238525 | G | A | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1145-1819G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108238525 | |||||||
chr12:108238698 | T | A | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1145-1646T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108238698 | |||||||
chr12:108238866 | G | A | 3 | a0003c0004t0026g0057 a0003c0004t0026g0058 a0003c0004t0068g0217 |
3 | HG02109.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1145-1478G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108238866 | |||||||
chr12:108239245 | C | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0013g0204 others(3): Show |
6 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1145-1099C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239245 | |||||||
chr12:108239281 | T | C | 28 | a0001c0001t0001g0149 a0001c0001t0001g0202 a0001c0001t0002g0137 others(25): Show |
29 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.1145-1063T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239281 | |||||||
chr12:108239486 | C | T | 1 | a0001c0001t0032g0004 | 2 | HG01257.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1145-858C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239486 | |||||||
chr12:108239515 | C | T | 1 | a0001c0001t0066g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1145-829C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239515 | |||||||
chr12:108239582 | C | T | 12 | a0001c0001t0011g0060 a0001c0001t0016g0047 a0001c0001t0016g0048 others(9): Show |
12 | HG01109.hp1 HG01943.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1145-762C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239582 | |||||||
chr12:108239719 | T | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0061g0266 |
4 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145-625T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239719 | |||||||
chr12:108239735 | G | A | 157 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(154): Show |
164 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1145-609G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239735 | |||||||
chr12:108239766 | C | G | 215 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(212): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1145-578C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239766 | |||||||
chr12:108239872 | C | A | 97 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(94): Show |
101 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1145-472C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239872 | |||||||
chr12:108239996 | C | G | 143 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(140): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1145-348C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239996 | |||||||
chr12:108240001 | G | A | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0013g0204 others(2): Show |
5 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145-343G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108240001 | |||||||
chr12:108240026 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1145-318C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108240026 | |||||||
chr12:108240091 | A | C | 1 | a0001c0001t0005g0255 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1145-253A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108240091 | |||||||
chr12:108240228 | C | T | 1 | a0002c0002t0019g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1145-116C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108240228 | |||||||
chr12:108240554 | G | C | 1 | a0001c0001t0066g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1345+10G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108240554 | |||||||
chr12:108240963 | T | C | 1 | a0007c0011t0004g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1345+419T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108240963 | |||||||
chr12:108241081 | A | G | 164 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(161): Show |
170 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1345+537A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241081 | |||||||
chr12:108241108 | ATCATTTC others(34): Show |
A | 1 | a0001c0001t0053g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1345+568_1345+608d others(43): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 108241108 | ||||||
chr12:108241319 | G | A | 14 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(11): Show |
15 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1345+775G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241319 | |||||||
chr12:108241455 | C | T | 165 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0081 others(162): Show |
171 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.1345+911C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241455 | |||||||
chr12:108241652 | C | A | 6 | a0001c0001t0036g0064 a0001c0003t0016g0059 a0001c0003t0022g0236 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345+1108C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241652 | |||||||
chr12:108241683 | G | A | 106 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0081 others(103): Show |
110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1345+1139G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241683 | |||||||
chr12:108241699 | T | C | 49 | a0001c0001t0002g0106 a0001c0001t0002g0141 a0001c0001t0002g0174 others(46): Show |
52 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1345+1155T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241699 | |||||||
chr12:108241723 | A | C | 1 | a0001c0001t0007g0053 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1345+1179A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241723 | |||||||
chr12:108241839 | G | A | 2 | a0001c0001t0008g0126 a0007c0011t0004g0099 |
2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1345+1295G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241839 | |||||||
chr12:108241868 | T | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1345+1324T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241868 | |||||||
chr12:108242004 | T | C | 1 | a0001c0001t0003g0244 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1345+1460T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242004 | |||||||
chr12:108242038 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0023g0146 others(2): Show |
6 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+1494G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242038 | |||||||
chr12:108242100 | G | A | 1 | a0003c0004t0026g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1345+1556G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242100 | |||||||
chr12:108242149 | G | C | 1 | a0001c0001t0011g0060 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1345+1605G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242149 | |||||||
chr12:108242155 | C | T | 4 | a0001c0001t0004g0121 a0001c0001t0012g0033 a0001c0001t0012g0036 others(1): Show |
4 | HG01943.hp1 HG02135.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345+1611C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242155 | |||||||
chr12:108242236 | T | A | 2 | a0001c0001t0008g0126 a0007c0011t0004g0099 |
2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1345+1692T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242236 | |||||||
chr12:108242293 | G | A | 46 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0202 others(43): Show |
48 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.1345+1749G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242293 | |||||||
chr12:108242384 | A | G | 1 | a0001c0010t0046g0230 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1345+1840A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242384 | |||||||
chr12:108242396 | G | T | 17 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(14): Show |
18 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.1345+1852G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242396 | |||||||
chr12:108242536 | A | G | 82 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0176 others(79): Show |
87 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1345+1992A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242536 | |||||||
chr12:108242544 | G | A | 8 | a0001c0001t0003g0260 a0001c0001t0007g0053 a0001c0001t0042g0223 others(5): Show |
8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1345+2000G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242544 | |||||||
chr12:108242555 | C | T | 3 | a0001c0001t0002g0174 a0001c0001t0005g0115 a0001c0001t0005g0116 |
3 | HG01257.hp2 HG01258.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1345+2011C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242555 | |||||||
chr12:108242606 | G | C | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1345+2062G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242606 | |||||||
chr12:108242654 | G | A | 2 | a0001c0001t0008g0126 a0007c0011t0004g0099 |
2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1345+2110G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242654 | |||||||
chr12:108242689 | G | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0002g0106 others(70): Show |
77 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1345+2145G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242689 | |||||||
chr12:108242789 | C | T | 3 | a0002c0002t0001g0140 a0002c0002t0001g0197 a0002c0002t0010g0195 |
3 | NA18945.hp1 NA18971.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1345+2245C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242789 | |||||||
chr12:108242843 | A | G | 110 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0098 others(107): Show |
116 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1345+2299A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242843 | |||||||
chr12:108242862 | C | T | 76 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0176 others(73): Show |
81 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1345+2318C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242862 | |||||||
chr12:108243117 | C | T | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1345+2573C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243117 | |||||||
chr12:108243118 | T | C | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1345+2574T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243118 | |||||||
chr12:108243120 | T | C | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1345+2576T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243120 | |||||||
chr12:108243124 | G | A | 17 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 others(14): Show |
18 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.1345+2580G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243124 | |||||||
chr12:108243151 | T | G | 3 | a0001c0001t0009g0043 a0001c0001t0025g0035 a0001c0001t0025g0046 |
3 | HG03490.hp2 HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1345+2607T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243151 | |||||||
chr12:108243255 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0023g0146 others(2): Show |
6 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+2711T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243255 | |||||||
chr12:108243330 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0176 others(71): Show |
79 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1345+2786C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243330 | |||||||
chr12:108243399 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1345+2855G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243399 | |||||||
chr12:108243439 | G | T | 1 | a0002c0002t0004g0073 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1345+2895G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243439 | |||||||
chr12:108243691 | C | T | 1 | a0001c0001t0030g0127 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1345+3147C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243691 | |||||||
chr12:108243727 | G | A | 3 | a0001c0003t0016g0059 a0001c0003t0031g0054 a0001c0003t0031g0055 |
3 | HG01243.hp2 HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1345+3183G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243727 | |||||||
chr12:108243792 | G | A | 6 | a0001c0001t0026g0039 a0001c0001t0034g0250 a0001c0001t0035g0070 others(3): Show |
6 | HG01891.hp1 HG01943.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345+3248G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243792 | |||||||
chr12:108243935 | A | G | 76 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0176 others(73): Show |
81 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1345+3391A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243935 | |||||||
chr12:108244145 | G | A | 1 | a0002c0002t0002g0261 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1345+3601G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244145 | |||||||
chr12:108244171 | G | T | 46 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0202 others(43): Show |
48 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.1345+3627G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244171 | |||||||
chr12:108244224 | G | A | 52 | a0001c0001t0002g0106 a0001c0001t0002g0141 a0001c0001t0002g0174 others(49): Show |
55 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1345+3680G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244224 | |||||||
chr12:108244386 | A | G | 6 | a0001c0001t0026g0039 a0001c0001t0034g0250 a0001c0001t0035g0070 others(3): Show |
6 | HG01891.hp1 HG01943.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-3605A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244386 | |||||||
chr12:108244409 | G | A | 1 | a0006c0006t0016g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1346-3582G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244409 | |||||||
chr12:108244469 | C | T | 2 | a0001c0001t0009g0052 a0001c0001t0054g0051 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1346-3522C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244469 | |||||||
chr12:108244582 | G | A | 1 | a0001c0001t0067g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1346-3409G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244582 | |||||||
chr12:108244604 | C | T | 1 | a0001c0001t0063g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1346-3387C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244604 | |||||||
chr12:108244636 | G | A | 1 | a0001c0001t0041g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1346-3355G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244636 | |||||||
chr12:108244659 | A | G | 1 | a0001c0001t0019g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1346-3332A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244659 | |||||||
chr12:108245137 | T | C | 2 | a0001c0001t0029g0226 a0001c0001t0029g0227 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1346-2854T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108245137 | |||||||
chr12:108245216 | G | A | 260 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(257): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1346-2775G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108245216 | |||||||
chr12:108245239 | C | CT | 103 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0098 others(100): Show |
109 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1346-2751dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 108245239 | ||||||
chr12:108245286 | A | G | 1 | a0001c0001t0009g0003 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1346-2705A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108245286 | |||||||
chr12:108245893 | A | G | 113 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0098 others(110): Show |
119 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1346-2098A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108245893 | |||||||
chr12:108245915 | C | T | 6 | a0001c0001t0001g0202 a0001c0001t0003g0138 a0001c0001t0007g0002 others(3): Show |
7 | HG00609.hp2 NA18944.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1346-2076C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108245915 | |||||||
chr12:108245951 | T | A | 2 | a0001c0001t0008g0012 a0001c0001t0040g0012 |
2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1346-2040T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108245951 | |||||||
chr12:108246096 | T | A | 1 | a0001c0001t0002g0077 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1346-1895T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246096 | |||||||
chr12:108246179 | C | T | 1 | a0001c0001t0008g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1346-1812C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246179 | |||||||
chr12:108246190 | C | T | 1 | a0001c0001t0012g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1346-1801C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246190 | |||||||
chr12:108246336 | C | T | 1 | a0001c0001t0018g0018 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1346-1655C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246336 | |||||||
chr12:108246388 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0245 a0001c0001t0023g0146 others(1): Show |
5 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-1603G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246388 | |||||||
chr12:108246402 | CTTGTGAG others(3): Show |
C | 2 | a0001c0001t0008g0126 a0007c0011t0004g0099 |
2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1346-1588_1346-157 others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246402 | |||||||
chr12:108246405 | G | A | 1 | a0001c0001t0056g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1346-1586G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246405 | |||||||
chr12:108246521 | C | G | 20 | a0001c0001t0001g0075 a0001c0001t0001g0218 a0001c0001t0001g0219 others(17): Show |
21 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1346-1470C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246521 | |||||||
chr12:108246536 | C | T | 1 | a0001c0001t0048g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1346-1455C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246536 | |||||||
chr12:108246537 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0004g0120 a0002c0002t0037g0078 |
3 | HG01978.hp1 HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1346-1454C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246537 | |||||||
chr12:108246686 | C | A | 1 | a0001c0001t0008g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1346-1305C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246686 | |||||||
chr12:108246687 | A | G | 2 | a0001c0001t0011g0060 a0001c0001t0015g0151 |
2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1346-1304A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246687 | |||||||
chr12:108246737 | AGAT | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0218 others(13): Show |
17 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1346-1247_1346-124 others(7): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 108246737 | ||||||
chr12:108246787 | C | T | 2 | a0001c0001t0036g0101 a0001c0001t0067g0063 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1346-1204C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246787 | |||||||
chr12:108246931 | T | C | 2 | a0002c0002t0001g0190 a0002c0002t0001g0203 |
2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1346-1060T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246931 | |||||||
chr12:108247000 | A | G | 1 | a0001c0001t0017g0094 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1346-991A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247000 | |||||||
chr12:108247014 | G | A | 263 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0076 others(260): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.1346-977G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247014 | |||||||
chr12:108247233 | G | A | 2 | a0001c0001t0041g0156 a0001c0001t0057g0251 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1346-758G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247233 | |||||||
chr12:108247352 | CAT | C | 6 | a0001c0001t0022g0087 a0001c0001t0036g0064 a0001c0001t0043g0147 others(3): Show |
6 | HG01109.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-637_1346-636d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 108247352 | ||||||
chr12:108247356 | A | G | 1 | a0001c0001t0022g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1346-635A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247356 | |||||||
chr12:108247533 | A | G | 1 | a0001c0001t0008g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1346-458A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247533 | |||||||
chr12:108247595 | A | T | 1 | a0007c0011t0004g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1346-396A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247595 | |||||||
chr12:108247814 | C | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG03688.hp1 HG03831.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1346-177C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247814 | |||||||
chr12:108247847 | T | A | 2 | a0001c0001t0001g0081 a0001c0001t0053g0024 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1346-144T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247847 | |||||||
chr12:108247954 | C | T | 1 | a0001c0003t0031g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1346-37C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247954 |