Item | Value |
---|---|
geneid | 23302 |
ensemblid | ENSG00000179314.16 |
hgncid | 29060 |
symbol | WSCD1 |
name | WSC domain containing 1 |
refseq_nuc | NM_015253.2 |
refseq_prot | NP_056068.1 |
ensembl_nuc | ENST00000317744.10 |
ensembl_prot | ENSP00000323087.5 |
mane_status | MANE Select |
chr | chr17 |
start | 6070379 |
end | 6124427 |
strand | + |
ver | v1.2 |
region | chr17:6070379-6124427 |
region5000 | chr17:6065379-6129427 |
regionname0 | WSCD1_chr17_6070379_6124427 |
regionname5000 | WSCD1_chr17_6065379_6129427 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 575 | 407 | 81 | 74 | 189 | 15 | 46 | 141 | WSCD1_chr17_6065379_6129427 | WSCD1 | MAKPF others(570): Show |
chr17 | 6065379 | 6129427 |
a0002 | 0/0 | 575 | 8 | 4 | 2 | 0 | 0 | 2 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | MAKPF others(570): Show |
chr17 | 6065379 | 6129427 |
a0003 | 0/0 | 575 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | MAKPF others(570): Show |
chr17 | 6065379 | 6129427 |
a0004 | 0/0 | 575 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | MAKPF others(570): Show |
chr17 | 6065379 | 6129427 |
a0005 | 0/0 | 575 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | MAKPF others(570): Show |
chr17 | 6065379 | 6129427 |
a0006 | 0/0 | 575 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | MAKPF others(570): Show |
chr17 | 6065379 | 6129427 |
a0007 | 0/0 | 575 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | MAKPF others(570): Show |
chr17 | 6065379 | 6129427 |
a0008 | 0/0 | 575 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | MAKPF others(570): Show |
chr17 | 6065379 | 6129427 |
a0009 | 0/0 | 575 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | MAKPF others(570): Show |
chr17 | 6065379 | 6129427 |
a0010 | 0/0 | 575 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | MAKPF others(570): Show |
chr17 | 6065379 | 6129427 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1725 | 232 | 9 | 36 | 148 | 10 | 28 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0001c0002 | 0/0 | 1725 | 131 | 55 | 31 | 28 | 5 | 12 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0001c0003 | 1/0 | 1725 | 18 | 12 | 2 | 2 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0001c0004 | 0/0 | 1725 | 16 | 5 | 2 | 8 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0001c0008 | 0/0 | 1725 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0001c0009 | 0/0 | 1725 | 2 | 0 | 1 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0001c0013 | 0/0 | 1725 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0001c0015 | 0/0 | 1725 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0001c0016 | 0/0 | 1725 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0001c0018 | 0/0 | 1725 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0001c0020 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0001c0023 | 0/0 | 1725 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0002c0006 | 0/0 | 1725 | 5 | 1 | 2 | 0 | 0 | 2 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0002c0007 | 0/0 | 1725 | 3 | 3 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0003c0005 | 0/0 | 1725 | 6 | 6 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0004c0010 | 0/0 | 1725 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0005c0021 | 0/0 | 1725 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0005c0022 | 0/0 | 1725 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0006c0014 | 0/0 | 1725 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0007c0017 | 0/0 | 1725 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0008c0012 | 0/0 | 1725 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0009c0019 | 0/0 | 1725 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 | ||
a0010c0011 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | ATGGC others(1720): Show |
chr17 | 6065379 | 6129427 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6056 | 75 | 1 | 9 | 55 | 3 | 7 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0002 | 0/0 | 6057 | 45 | 0 | 2 | 36 | 1 | 6 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0003 | 0/0 | 6057 | 27 | 0 | 10 | 10 | 1 | 6 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0004 | 0/0 | 6057 | 3 | 1 | 0 | 0 | 1 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0005 | 0/0 | 6057 | 10 | 0 | 4 | 5 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0006 | 0/0 | 6057 | 9 | 0 | 0 | 9 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0007 | 0/0 | 6057 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0008 | 0/0 | 6057 | 4 | 0 | 2 | 1 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0009 | 0/1 | 6057 | 2 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0010 | 0/0 | 6057 | 3 | 0 | 0 | 3 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0011 | 0/0 | 6056 | 4 | 0 | 2 | 2 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0012 | 0/0 | 6057 | 3 | 0 | 2 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0019 | 0/0 | 6057 | 4 | 0 | 1 | 3 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0021 | 0/0 | 6057 | 4 | 0 | 0 | 4 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0024 | 0/0 | 6057 | 3 | 0 | 0 | 2 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0027 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0028 | 0/0 | 6056 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0030 | 0/0 | 6057 | 2 | 0 | 1 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0033 | 0/0 | 6056 | 2 | 0 | 0 | 0 | 2 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0034 | 0/0 | 6057 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0035 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0036 | 0/0 | 6057 | 2 | 0 | 0 | 0 | 0 | 2 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0037 | 0/0 | 6057 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0038 | 0/0 | 6057 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0039 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0045 | 0/0 | 6057 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0047 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0048 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0050 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0053 | 0/0 | 6056 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0058 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0059 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0060 | 0/0 | 6056 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0063 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0064 | 0/0 | 6056 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0065 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0066 | 0/0 | 6023 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6018): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0069 | 0/0 | 6057 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0071 | 0/0 | 6056 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0080 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0083 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0084 | 0/0 | 6056 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0001t0088 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0001 | 0/0 | 6056 | 27 | 2 | 8 | 11 | 2 | 4 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0002 | 0/0 | 6057 | 9 | 0 | 3 | 3 | 1 | 2 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0003 | 0/0 | 6057 | 6 | 0 | 2 | 1 | 0 | 3 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0004 | 0/0 | 6057 | 9 | 7 | 1 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0005 | 0/0 | 6057 | 4 | 0 | 3 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0006 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0007 | 0/0 | 6057 | 4 | 4 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0008 | 0/0 | 6057 | 5 | 0 | 5 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0009 | 0/0 | 6057 | 6 | 0 | 6 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0010 | 0/0 | 6057 | 3 | 0 | 0 | 3 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0011 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0012 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0013 | 0/0 | 6057 | 5 | 5 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0014 | 0/0 | 6057 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0015 | 0/0 | 6057 | 4 | 4 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0016 | 0/0 | 6056 | 4 | 0 | 0 | 4 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0017 | 0/0 | 6057 | 3 | 3 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0018 | 0/0 | 6057 | 2 | 1 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0020 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0022 | 0/0 | 6057 | 3 | 3 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0023 | 0/0 | 6057 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0025 | 0/0 | 6057 | 3 | 3 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0026 | 0/0 | 6057 | 3 | 3 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0029 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0031 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0032 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0039 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0042 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0043 | 0/0 | 6056 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0049 | 0/0 | 6057 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0051 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0052 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0054 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0055 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0057 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0062 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0067 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0070 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0072 | 0/0 | 6057 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0075 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0077 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0078 | 0/0 | 6056 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0081 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0085 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0087 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0002t0091 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0001 | 0/0 | 6056 | 3 | 0 | 1 | 2 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0004 | 0/0 | 6057 | 3 | 3 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0007 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0012 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0014 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0017 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0029 | 1/0 | 6056 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0031 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0035 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0044 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0046 | 0/0 | 6057 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0076 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0089 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0003t0092 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0001 | 0/0 | 6056 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0002 | 0/0 | 6057 | 3 | 0 | 1 | 2 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0003 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0004 | 0/0 | 6057 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0007 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0011 | 0/0 | 6056 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0014 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0027 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0032 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0041 | 0/0 | 6056 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0068 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0073 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0004t0082 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0008t0002 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0008t0028 | 0/0 | 6056 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0009t0001 | 0/0 | 6056 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0009t0003 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0013t0004 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0015t0061 | 0/0 | 6056 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0001c0016t0003 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0018t0018 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0020t0003 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0001c0023t0001 | 0/0 | 6056 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0002c0006t0002 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0002c0006t0005 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0002c0006t0007 | 0/0 | 6057 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0002c0006t0015 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0002c0006t0056 | 0/0 | 6057 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0002c0007t0003 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0002c0007t0023 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0002c0007t0090 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0003c0005t0014 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0003c0005t0020 | 0/0 | 6056 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0003c0005t0022 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0003c0005t0074 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0003c0005t0079 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0004c0010t0040 | 0/0 | 6056 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0005c0021t0004 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0005c0022t0020 | 0/0 | 6056 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6051): Show |
chr17 | 6065379 | 6129427 |
a0006c0014t0005 | 0/0 | 6057 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0007c0017t0018 | 0/0 | 6057 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0008c0012t0086 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0009c0019t0002 | 0/0 | 6057 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
a0010c0011t0002 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | GCAGA others(6052): Show |
chr17 | 6065379 | 6129427 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0001g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0002g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0397 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0003g0398 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0005g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0005g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0006g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0006g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0006g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0006g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0008g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0008g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0008g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0008g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0009g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0009g0401 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0010g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0010g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0010g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0011g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0011g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0011g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0012g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0012g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0012g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0019g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0019g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0019g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0019g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0021g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0021g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0021g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0021g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0024g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0024g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0024g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0027g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0028g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0030g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0030g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0033g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0033g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0034g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0034g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0035g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0036g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0036g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0037g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0037g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0038g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0038g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0039g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0045g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0047g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0048g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0050g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0053g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0058g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0059g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0060g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0063g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0064g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0065g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0066g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0069g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0071g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0080g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0083g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0084g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0001t0088g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0003g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0004g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0004g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0004g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0004g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0007g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0007g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0008g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0008g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0008g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0009g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0009g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0009g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0009g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0010g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0010g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0010g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0011g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0012g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0013g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0013g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0013g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0014g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0015g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0015g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0015g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0016g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0016g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0016g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0016g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0017g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0017g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0017g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0018g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0018g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0020g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0022g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0022g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0022g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0023g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0023g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0025g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0025g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0025g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0026g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0026g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0026g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0029g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0031g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0032g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0039g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0042g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0043g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0049g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0051g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0052g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0054g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0055g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0057g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0062g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0067g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0070g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0072g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0075g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0077g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0078g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0081g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0085g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0087g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0002t0091g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0012g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0014g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0017g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0029g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0031g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0035g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0044g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0046g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0076g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0089g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0003t0092g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0011g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0014g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0027g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0032g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0041g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0068g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0073g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0004t0082g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0008t0002g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0008t0028g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0009t0001g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0009t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0013t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0015t0061g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0016t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0018t0018g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0020t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0001c0023t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0002c0006t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0002c0006t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0002c0006t0007g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0002c0006t0015g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0002c0006t0056g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0002c0007t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0002c0007t0023g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0002c0007t0090g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0003c0005t0014g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0003c0005t0020g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0003c0005t0020g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0003c0005t0022g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0003c0005t0074g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0003c0005t0079g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0004c0010t0040g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0004c0010t0040g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0005c0021t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0005c0022t0020g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0006c0014t0005g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0007c0017t0018g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0008c0012t0086g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0009c0019t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
a0010c0011t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0007 | EUR | GBR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00099 | hp2 | a0006 | c0014 | t0005 | g0019 | EUR | GBR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0222 | EUR | FIN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0142 | EUR | FIN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00323 | hp1 | a0001 | c0002 | t0005 | g0231 | EUR | FIN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0303 | EUR | FIN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00408 | hp1 | a0001 | c0008 | t0002 | g0396 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00408 | hp2 | a0001 | c0001 | t0027 | g0277 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00423 | hp1 | a0001 | c0008 | t0028 | g0306 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00423 | hp2 | a0001 | c0002 | t0016 | g0332 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00544 | hp1 | a0001 | c0004 | t0002 | g0288 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00597 | hp1 | a0001 | c0001 | t0006 | g0392 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00597 | hp2 | a0001 | c0001 | t0083 | g0297 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00621 | hp1 | a0001 | c0020 | t0003 | g0138 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00639 | hp2 | a0001 | c0002 | t0008 | g0260 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0340 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00733 | hp1 | a0001 | c0002 | t0009 | g0224 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00735 | hp1 | a0001 | c0001 | t0011 | g0023 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00735 | hp2 | a0001 | c0002 | t0004 | g0342 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00738 | hp1 | a0001 | c0001 | t0019 | g0055 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0388 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00741 | hp1 | a0001 | c0001 | t0037 | g0348 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01069 | hp2 | a0001 | c0001 | t0012 | g0215 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01070 | hp1 | a0002 | c0006 | t0056 | g0110 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01074 | hp1 | a0001 | c0002 | t0009 | g0018 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01074 | hp2 | a0001 | c0002 | t0008 | g0020 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0031 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01081 | hp2 | a0001 | c0002 | t0009 | g0229 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01099 | hp2 | a0001 | c0002 | t0005 | g0212 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0236 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01109 | hp1 | a0001 | c0001 | t0012 | g0198 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01109 | hp2 | a0002 | c0006 | t0007 | g0166 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01167 | hp1 | a0001 | c0002 | t0049 | g0366 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01168 | hp1 | a0001 | c0002 | t0008 | g0020 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0347 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01169 | hp2 | a0001 | c0002 | t0008 | g0246 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0397 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01243 | hp1 | a0001 | c0002 | t0072 | g0262 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01243 | hp2 | a0001 | c0002 | t0078 | g0384 | AMR | PUR | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0220 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01256 | hp2 | a0001 | c0004 | t0002 | g0337 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01257 | hp2 | a0001 | c0004 | t0041 | g0120 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0228 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01261 | hp2 | a0001 | c0009 | t0001 | g0394 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0210 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01346 | hp2 | a0001 | c0001 | t0030 | g0322 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01358 | hp2 | a0001 | c0002 | t0008 | g0247 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0311 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01361 | hp2 | a0001 | c0003 | t0046 | g0029 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01433 | hp2 | a0001 | c0023 | t0001 | g0026 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01496 | hp1 | a0007 | c0017 | t0018 | g0211 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01496 | hp2 | a0001 | c0001 | t0008 | g0286 | AMR | CLM | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0346 | EUR | IBS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01516 | hp1 | a0001 | c0001 | t0033 | g0122 | EUR | IBS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01517 | hp2 | a0001 | c0001 | t0033 | g0121 | EUR | IBS | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01884 | hp1 | a0001 | c0002 | t0022 | g0047 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01884 | hp2 | a0001 | c0004 | t0004 | g0172 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01891 | hp1 | a0001 | c0004 | t0007 | g0164 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01891 | hp2 | a0001 | c0002 | t0091 | g0201 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01943 | hp2 | a0001 | c0015 | t0061 | g0027 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01952 | hp1 | a0001 | c0001 | t0011 | g0312 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01952 | hp2 | a0001 | c0002 | t0003 | g0248 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01975 | hp1 | a0001 | c0001 | t0069 | g0209 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01978 | hp1 | a0001 | c0002 | t0009 | g0003 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01981 | hp1 | a0001 | c0002 | t0005 | g0025 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01981 | hp2 | a0001 | c0002 | t0009 | g0003 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02004 | hp1 | a0001 | c0001 | t0045 | g0123 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02015 | hp1 | a0001 | c0001 | t0006 | g0109 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0369 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0319 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0328 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02055 | hp1 | a0001 | c0002 | t0004 | g0389 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02055 | hp2 | a0001 | c0002 | t0004 | g0374 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02071 | hp1 | a0001 | c0001 | t0058 | g0133 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0218 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0399 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0330 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0364 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02083 | hp1 | a0001 | c0001 | t0008 | g0295 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0351 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0370 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02135 | hp1 | a0001 | c0001 | t0005 | g0289 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0393 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02145 | hp1 | a0002 | c0007 | t0003 | g0168 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0227 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02148 | hp2 | a0001 | c0001 | t0008 | g0259 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0362 | EAS | CDX | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0350 | EAS | CDX | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | CDX | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CDX | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02257 | hp1 | a0008 | c0012 | t0086 | g0283 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02257 | hp2 | a0004 | c0010 | t0040 | g0043 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02258 | hp1 | a0001 | c0002 | t0004 | g0041 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02258 | hp2 | a0001 | c0004 | t0004 | g0187 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02273 | hp1 | a0001 | c0002 | t0009 | g0018 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02280 | hp1 | a0003 | c0005 | t0022 | g0344 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02280 | hp2 | a0001 | c0002 | t0029 | g0190 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02300 | hp1 | a0009 | c0019 | t0002 | g0033 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02300 | hp2 | a0001 | c0002 | t0005 | g0139 | AMR | PEL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02451 | hp1 | a0001 | c0002 | t0014 | g0375 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02451 | hp2 | a0001 | c0002 | t0004 | g0191 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02523 | hp1 | a0001 | c0001 | t0006 | g0314 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02572 | hp1 | a0001 | c0002 | t0022 | g0254 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02572 | hp2 | a0001 | c0003 | t0076 | g0378 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02602 | hp1 | a0002 | c0006 | t0005 | g0159 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02615 | hp1 | a0001 | c0002 | t0062 | g0173 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02615 | hp2 | a0001 | c0002 | t0026 | g0200 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02622 | hp1 | a0001 | c0002 | t0017 | g0179 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02622 | hp2 | a0001 | c0002 | t0023 | g0188 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02630 | hp1 | a0001 | c0004 | t0073 | g0386 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02630 | hp2 | a0001 | c0003 | t0004 | g0195 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02647 | hp1 | a0002 | c0007 | t0090 | g0184 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02647 | hp2 | a0001 | c0004 | t0014 | g0170 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0339 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02698 | hp2 | a0001 | c0002 | t0087 | g0293 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02717 | hp1 | a0001 | c0002 | t0057 | g0338 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02717 | hp2 | a0001 | c0002 | t0023 | g0243 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02723 | hp1 | a0001 | c0001 | t0088 | g0282 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0341 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02735 | hp1 | a0001 | c0001 | t0012 | g0088 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02738 | hp1 | a0001 | c0002 | t0003 | g0336 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02809 | hp1 | a0001 | c0002 | t0014 | g0171 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02809 | hp2 | a0001 | c0002 | t0018 | g0214 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02818 | hp1 | a0001 | c0002 | t0004 | g0377 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02818 | hp2 | a0001 | c0002 | t0007 | g0185 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02886 | hp1 | a0001 | c0002 | t0004 | g0316 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02886 | hp2 | a0001 | c0002 | t0015 | g0036 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02895 | hp1 | a0001 | c0002 | t0052 | g0169 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02895 | hp2 | a0001 | c0002 | t0025 | g0352 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02896 | hp1 | a0001 | c0002 | t0025 | g0353 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02896 | hp2 | a0001 | c0002 | t0075 | g0181 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02922 | hp1 | a0001 | c0002 | t0081 | g0376 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02922 | hp2 | a0003 | c0005 | t0014 | g0193 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02965 | hp1 | a0001 | c0003 | t0089 | g0203 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02965 | hp2 | a0001 | c0002 | t0013 | g0009 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02970 | hp1 | a0001 | c0003 | t0035 | g0245 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02970 | hp2 | a0001 | c0003 | t0007 | g0326 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02976 | hp1 | a0001 | c0002 | t0031 | g0015 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02976 | hp2 | a0001 | c0002 | t0013 | g0091 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0099 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0051 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03041 | hp1 | a0001 | c0003 | t0004 | g0194 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03041 | hp2 | a0001 | c0002 | t0042 | g0207 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03098 | hp1 | a0001 | c0002 | t0025 | g0383 | AFR | MSL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03098 | hp2 | a0001 | c0002 | t0022 | g0255 | AFR | MSL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0044 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03130 | hp2 | a0003 | c0005 | t0020 | g0343 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03139 | hp1 | a0001 | c0002 | t0015 | g0037 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03139 | hp2 | a0003 | c0005 | t0074 | g0387 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03195 | hp1 | a0001 | c0002 | t0026 | g0204 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03195 | hp2 | a0001 | c0002 | t0013 | g0009 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03209 | hp1 | a0001 | c0002 | t0020 | g0192 | AFR | MSL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03209 | hp2 | a0001 | c0002 | t0077 | g0381 | AFR | MSL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03239 | hp1 | a0001 | c0002 | t0004 | g0182 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03239 | hp2 | a0001 | c0004 | t0082 | g0258 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03453 | hp1 | a0001 | c0003 | t0044 | g0333 | AFR | MSL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03453 | hp2 | a0001 | c0003 | t0092 | g0202 | AFR | MSL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03486 | hp1 | a0005 | c0022 | t0020 | g0155 | AFR | MSL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03486 | hp2 | a0001 | c0002 | t0007 | g0242 | AFR | MSL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0149 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03491 | hp2 | a0001 | c0001 | t0036 | g0089 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03492 | hp1 | a0001 | c0001 | t0036 | g0113 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03516 | hp1 | a0001 | c0002 | t0085 | g0284 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03516 | hp2 | a0005 | c0021 | t0004 | g0154 | AFR | ESN | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03540 | hp1 | a0001 | c0002 | t0007 | g0334 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03540 | hp2 | a0002 | c0007 | t0023 | g0038 | AFR | GWD | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03579 | hp1 | a0001 | c0002 | t0070 | g0354 | AFR | MSL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03579 | hp2 | a0001 | c0001 | t0080 | g0382 | AFR | MSL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03654 | hp1 | a0001 | c0001 | t0008 | g0251 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03654 | hp2 | a0001 | c0001 | t0024 | g0197 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03669 | hp1 | a0001 | c0003 | t0012 | g0263 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03688 | hp1 | a0001 | c0013 | t0004 | g0217 | SAS | STU | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03688 | hp2 | a0001 | c0002 | t0018 | g0380 | SAS | STU | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03710 | hp1 | a0001 | c0001 | t0065 | g0114 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0398 | SAS | PJL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | BEB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03831 | hp2 | a0001 | c0001 | t0009 | g0401 | SAS | BEB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03834 | hp2 | a0001 | c0001 | t0050 | g0250 | SAS | BEB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0084 | SAS | BEB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | BEB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | BEB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0065 | SAS | BEB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG04184 | hp2 | a0001 | c0009 | t0003 | g0013 | SAS | BEB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG04199 | hp1 | a0001 | c0002 | t0003 | g0177 | SAS | STU | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0147 | SAS | STU | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | STU | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG04204 | hp2 | a0002 | c0006 | t0002 | g0028 | SAS | STU | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG04228 | hp1 | a0001 | c0018 | t0018 | g0335 | SAS | STU | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0090 | SAS | STU | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18522 | hp1 | a0001 | c0002 | t0054 | g0379 | AFR | YRI | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18522 | hp2 | a0001 | c0002 | t0026 | g0205 | AFR | YRI | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18747 | hp1 | a0001 | c0004 | t0001 | g0072 | EAS | CHB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | CHB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18906 | hp1 | a0001 | c0002 | t0051 | g0186 | AFR | YRI | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18906 | hp2 | a0001 | c0003 | t0014 | g0256 | AFR | YRI | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18939 | hp2 | a0001 | c0001 | t0034 | g0097 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18940 | hp1 | a0001 | c0002 | t0016 | g0360 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18940 | hp2 | a0001 | c0001 | t0010 | g0267 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18943 | hp1 | a0001 | c0001 | t0019 | g0136 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18943 | hp2 | a0001 | c0002 | t0010 | g0093 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18944 | hp1 | a0001 | c0001 | t0064 | g0160 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18945 | hp1 | a0001 | c0001 | t0021 | g0021 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18946 | hp2 | a0001 | c0004 | t0011 | g0271 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18947 | hp1 | a0001 | c0001 | t0006 | g0367 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0395 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18950 | hp1 | a0001 | c0001 | t0063 | g0307 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18953 | hp1 | a0001 | c0002 | t0003 | g0233 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0391 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18957 | hp2 | a0001 | c0001 | t0010 | g0323 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18960 | hp2 | a0001 | c0001 | t0038 | g0068 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18961 | hp2 | a0001 | c0002 | t0043 | g0359 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18962 | hp1 | a0001 | c0001 | t0019 | g0304 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18962 | hp2 | a0001 | c0002 | t0010 | g0176 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18963 | hp1 | a0001 | c0004 | t0027 | g0276 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18964 | hp1 | a0001 | c0001 | t0006 | g0131 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18967 | hp1 | a0001 | c0002 | t0016 | g0363 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18967 | hp2 | a0001 | c0001 | t0005 | g0305 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18968 | hp1 | a0001 | c0001 | t0021 | g0075 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18969 | hp2 | a0001 | c0004 | t0003 | g0308 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18970 | hp1 | a0001 | c0002 | t0010 | g0318 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18971 | hp1 | a0001 | c0001 | t0010 | g0135 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18973 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18977 | hp2 | a0001 | c0001 | t0019 | g0150 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18979 | hp1 | a0001 | c0001 | t0059 | g0070 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18988 | hp2 | a0001 | c0001 | t0028 | g0265 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18989 | hp1 | a0001 | c0002 | t0016 | g0358 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0390 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18991 | hp2 | a0001 | c0001 | t0060 | g0252 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18992 | hp1 | a0001 | c0002 | t0032 | g0106 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0400 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19007 | hp1 | a0001 | c0001 | t0011 | g0134 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19007 | hp2 | a0001 | c0001 | t0071 | g0098 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0402 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19010 | hp1 | a0001 | c0001 | t0024 | g0178 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19010 | hp2 | a0001 | c0001 | t0066 | g0077 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19011 | hp1 | a0001 | c0004 | t0002 | g0011 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19011 | hp2 | a0001 | c0001 | t0024 | g0274 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19012 | hp2 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19030 | hp1 | a0001 | c0001 | t0035 | g0035 | AFR | LWK | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19030 | hp2 | a0001 | c0002 | t0013 | g0165 | AFR | LWK | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19043 | hp1 | a0001 | c0002 | t0013 | g0049 | AFR | LWK | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19043 | hp2 | a0001 | c0001 | t0048 | g0349 | AFR | LWK | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19054 | hp1 | a0001 | c0001 | t0047 | g0086 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19054 | hp2 | a0010 | c0011 | t0002 | g0291 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19055 | hp1 | a0001 | c0002 | t0006 | g0294 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19060 | hp1 | a0001 | c0001 | t0006 | g0273 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19063 | hp2 | a0001 | c0001 | t0038 | g0060 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19064 | hp1 | a0001 | c0002 | t0067 | g0175 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19065 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19065 | hp2 | a0001 | c0002 | t0055 | g0152 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19066 | hp1 | a0001 | c0001 | t0021 | g0148 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19066 | hp2 | a0001 | c0001 | t0039 | g0146 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19077 | hp2 | a0001 | c0001 | t0034 | g0008 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19081 | hp2 | a0001 | c0002 | t0039 | g0253 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19083 | hp2 | a0001 | c0001 | t0006 | g0157 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19084 | hp2 | a0001 | c0001 | t0021 | g0257 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19085 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19085 | hp2 | a0001 | c0004 | t0068 | g0011 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19087 | hp1 | a0001 | c0001 | t0084 | g0299 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19088 | hp2 | a0001 | c0001 | t0053 | g0234 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19089 | hp2 | a0001 | c0004 | t0032 | g0371 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19240 | hp1 | a0001 | c0003 | t0004 | g0189 | AFR | YRI | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA19240 | hp2 | a0002 | c0006 | t0015 | g0111 | AFR | YRI | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA20129 | hp1 | a0003 | c0005 | t0079 | g0385 | AFR | ASW | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | ASW | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0101 | EUR | TSI | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA20752 | hp2 | a0001 | c0002 | t0012 | g0223 | EUR | TSI | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0232 | EUR | TSI | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA20805 | hp2 | a0001 | c0001 | t0030 | g0100 | EUR | TSI | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | GIH | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA20905 | hp2 | a0001 | c0016 | t0003 | g0230 | SAS | GIH | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02109 | hp2 | a0001 | c0002 | t0015 | g0054 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02486 | hp1 | a0001 | c0002 | t0015 | g0174 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02486 | hp2 | a0003 | c0005 | t0020 | g0345 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02559 | hp1 | a0001 | c0002 | t0017 | g0015 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG02559 | hp2 | a0001 | c0002 | t0004 | g0167 | AFR | ACB | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03471 | hp1 | a0001 | c0003 | t0031 | g0206 | AFR | MSL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0320 | AFR | MSL | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG06807 | hp1 | a0001 | c0002 | t0017 | g0163 | AFR | USA | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
HG06807 | hp2 | a0001 | c0002 | t0007 | g0244 | AFR | USA | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA20300 | hp1 | a0004 | c0010 | t0040 | g0042 | AFR | USA | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA20300 | hp2 | a0001 | c0002 | t0011 | g0225 | AFR | USA | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA21309 | hp1 | a0001 | c0003 | t0017 | g0365 | AFR | LWK | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
NA21309 | hp2 | a0001 | c0001 | t0037 | g0180 | AFR | LWK | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0085 | REF | REF | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
homoSapiens | grch38p0 | a0001 | c0003 | t0029 | g0039 | REF | REF | WSCD1_chr17_6065379_6129427 | WSCD1 | chr17 | 6065379 | 6129427 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:6080776 | G | A | 1 | a0010 | 1 | NA19054.hp2 | missense_variant | MODERATE | c.118G>A | p.Val40Met | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/9 | 680/6056 | 118/1728 | 40/575 | chr17 | 6080776 | |||
chr17:6080999 | G | A | 1 | a0008 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.341G>A | p.Arg114His | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/9 | 903/6056 | 341/1728 | 114/575 | chr17 | 6080999 | |||
chr17:6081038 | C | T | 1 | a0005 | 2 | HG03486.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.380C>T | p.Pro127Leu | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/9 | 942/6056 | 380/1728 | 127/575 | chr17 | 6081038 | |||
chr17:6088017 | A | C | 2 | a0003 a0004 |
8 | HG02257.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
missense_variant | MODERATE | c.455A>C | p.Asp152Ala | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/9 | 1017/6056 | 455/1728 | 152/575 | chr17 | 6088017 | |||
chr17:6109659 | C | T | 1 | a0007 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.902C>T | p.Thr301Ile | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 6/9 | 1464/6056 | 902/1728 | 301/575 | chr17 | 6109659 | |||
chr17:6109664 | C | T | 1 | a0009 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.907C>T | p.Arg303Trp | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 6/9 | 1469/6056 | 907/1728 | 303/575 | chr17 | 6109664 | |||
chr17:6110921 | C | A | 1 | a0006 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.1160C>A | p.Thr387Asn | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/9 | 1722/6056 | 1160/1728 | 387/575 | chr17 | 6110921 | |||
chr17:6118035 | G | A | 1 | a0002 | 8 | HG01070.hp1 HG01109.hp2 HG02145.hp1 others(5): Show |
missense_variant | MODERATE | c.1222G>A | p.Val408Ile | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/9 | 1784/6056 | 1222/1728 | 408/575 | chr17 | 6118035 | |||
chr17:6120536 | T | C | 1 | a0004 | 2 | HG02257.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.1603T>C | p.Ser535Pro | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2165/6056 | 1603/1728 | 535/575 | chr17 | 6120536 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:6080835 | C | T | 1 | a0001c0023 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.177C>T | p.Ala59Ala | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/9 | 739/6056 | 177/1728 | 59/575 | chr17 | 6080835 | |||
chr17:6080994 | G | A | 1 | a0001c0008 | 2 | HG00408.hp1 HG00423.hp1 |
synonymous_variant | LOW | c.336G>A | p.Leu112Leu | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/9 | 898/6056 | 336/1728 | 112/575 | chr17 | 6080994 | |||
chr17:6088024 | C | T | 10 | a0001c0001 a0001c0004 a0001c0008 others(7): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(258): Show |
synonymous_variant | LOW | c.462C>T | p.His154His | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/9 | 1024/6056 | 462/1728 | 154/575 | chr17 | 6088024 | |||
chr17:6090480 | C | T | 1 | a0001c0020 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.702C>T | p.Asp234Asp | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/9 | 1264/6056 | 702/1728 | 234/575 | chr17 | 6090480 | |||
chr17:6109750 | C | T | 1 | a0001c0016 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.993C>T | p.Tyr331Tyr | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 6/9 | 1555/6056 | 993/1728 | 331/575 | chr17 | 6109750 | |||
chr17:6110856 | A | G | 17 | a0001c0001 a0001c0002 a0001c0008 others(14): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
synonymous_variant | LOW | c.1095A>G | p.Thr365Thr | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/9 | 1657/6056 | 1095/1728 | 365/575 | chr17 | 6110856 | |||
chr17:6110868 | C | T | 1 | a0001c0018 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1107C>T | p.His369His | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/9 | 1669/6056 | 1107/1728 | 369/575 | chr17 | 6110868 | |||
chr17:6120472 | C | T | 3 | a0001c0009 a0001c0013 a0001c0015 |
4 | HG01261.hp2 HG01943.hp2 HG03688.hp1 others(1): Show |
synonymous_variant | LOW | c.1539C>T | p.Ser513Ser | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2101/6056 | 1539/1728 | 513/575 | chr17 | 6120472 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:6070429 | C | G | 5 | a0001c0002t0026 a0001c0002t0091 a0001c0003t0089 others(2): Show |
7 | HG01891.hp2 HG02615.hp2 HG02647.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-512C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/9 | 10230 | chr17 | 6070429 | ||||||
chr17:6070490 | G | C | 1 | a0001c0004t0041 | 1 | HG01257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-451G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/9 | 10169 | chr17 | 6070490 | ||||||
chr17:6070542 | G | T | 10 | a0001c0001t0008 a0001c0001t0083 a0001c0001t0084 others(7): Show |
18 | HG00597.hp2 HG00639.hp2 HG01074.hp2 others(15): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-399G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/9 | chr17 | 6070542 | |||||||
chr17:6070551 | G | A | 2 | a0001c0001t0027 a0001c0004t0027 |
2 | HG00408.hp2 NA18963.hp1 |
5_prime_UTR_variant | MODIFIER | c.-390G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/9 | 10108 | chr17 | 6070551 | ||||||
chr17:6070590 | G | C | 1 | a0001c0002t0042 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-351G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/9 | 10069 | chr17 | 6070590 | ||||||
chr17:6070605 | C | T | 1 | a0001c0002t0081 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-336C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/9 | 10054 | chr17 | 6070605 | ||||||
chr17:6070610 | C | T | 5 | a0001c0001t0080 a0001c0002t0025 a0001c0002t0077 others(2): Show |
7 | HG01243.hp2 HG02895.hp2 HG02896.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-331C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/9 | 10049 | chr17 | 6070610 | ||||||
chr17:6080377 | G | C | 2 | a0001c0002t0016 a0001c0002t0043 |
5 | HG00423.hp2 NA18940.hp1 NA18961.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-282G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/9 | 282 | chr17 | 6080377 | ||||||
chr17:6080395 | C | T | 3 | a0001c0002t0075 a0001c0002t0081 a0001c0003t0076 |
3 | HG02572.hp2 HG02896.hp2 HG02922.hp1 |
5_prime_UTR_variant | MODIFIER | c.-264C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/9 | 264 | chr17 | 6080395 | ||||||
chr17:6080550 | C | T | 3 | a0001c0002t0072 a0001c0004t0073 a0003c0005t0074 |
3 | HG01243.hp1 HG02630.hp1 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-109C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/9 | 109 | chr17 | 6080550 | ||||||
chr17:6080609 | C | T | 1 | a0001c0001t0088 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-50C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/9 | 50 | chr17 | 6080609 | ||||||
chr17:6080653 | A | C | 1 | a0001c0001t0071 | 1 | NA19007.hp2 | 5_prime_UTR_variant | MODIFIER | c.-6A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/9 | 6 | chr17 | 6080653 | ||||||
chr17:6120675 | C | T | 2 | a0001c0001t0039 a0001c0002t0039 |
2 | NA19066.hp2 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*14C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 14 | chr17 | 6120675 | ||||||
chr17:6120682 | G | A | 3 | a0001c0001t0045 a0001c0003t0044 a0001c0003t0046 |
3 | HG01361.hp2 HG02004.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*21G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 21 | chr17 | 6120682 | ||||||
chr17:6120683 | C | T | 1 | a0001c0002t0070 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 22 | chr17 | 6120683 | ||||||
chr17:6120771 | G | T | 1 | a0001c0002t0087 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*110G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 110 | chr17 | 6120771 | ||||||
chr17:6120868 | C | T | 7 | a0001c0001t0009 a0001c0001t0069 a0001c0001t0080 others(4): Show |
15 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*207C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 207 | chr17 | 6120868 | ||||||
chr17:6120968 | A | C | 31 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(28): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*307A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 307 | chr17 | 6120968 | ||||||
chr17:6121009 | G | A | 1 | a0001c0003t0044 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*348G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 348 | chr17 | 6121009 | ||||||
chr17:6121134 | C | G | 3 | a0001c0002t0062 a0001c0002t0085 a0001c0003t0044 |
3 | HG02615.hp1 HG03453.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*473C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 473 | chr17 | 6121134 | ||||||
chr17:6121150 | G | T | 1 | a0003c0005t0079 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*489G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 489 | chr17 | 6121150 | ||||||
chr17:6121232 | G | A | 4 | a0001c0001t0047 a0001c0001t0080 a0001c0002t0015 others(1): Show |
7 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*571G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 571 | chr17 | 6121232 | ||||||
chr17:6121373 | G | T | 25 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0021 others(22): Show |
139 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*712G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 712 | chr17 | 6121373 | ||||||
chr17:6121466 | G | T | 66 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(63): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*805G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 805 | chr17 | 6121466 | ||||||
chr17:6121683 | G | A | 9 | a0001c0001t0012 a0001c0001t0035 a0001c0001t0045 others(6): Show |
13 | HG01069.hp2 HG01109.hp1 HG02004.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1022G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1022 | chr17 | 6121683 | ||||||
chr17:6121707 | C | T | 1 | a0001c0015t0061 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1046C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1046 | chr17 | 6121707 | ||||||
chr17:6121759 | TAGTA | T | 108 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(105): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*1099_*1102delAGTA | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1099 | chr17 | 6121759 | ||||||
chr17:6121766 | C | CATGAG | 108 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(105): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*1106_*1107insTGAG others(1): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1107 | INFO_REALIGN_3_PRIME | chr17 | 6121766 | |||||
chr17:6121770 | C | A | 108 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(105): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*1109C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1109 | chr17 | 6121770 | ||||||
chr17:6121771 | T | G | 108 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(105): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*1110T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1110 | chr17 | 6121771 | ||||||
chr17:6121796 | C | T | 2 | a0001c0002t0062 a0001c0002t0085 |
2 | HG02615.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1135C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1135 | chr17 | 6121796 | ||||||
chr17:6121804 | G | A | 28 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0012 others(25): Show |
48 | HG00733.hp1 HG01069.hp2 HG01074.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1143G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1143 | chr17 | 6121804 | ||||||
chr17:6121900 | C | T | 5 | a0001c0002t0052 a0001c0002t0054 a0001c0002t0075 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1239C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1239 | chr17 | 6121900 | ||||||
chr17:6121913 | C | A | 4 | a0001c0001t0088 a0001c0002t0020 a0003c0005t0020 others(1): Show |
5 | HG02486.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1252C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1252 | chr17 | 6121913 | ||||||
chr17:6122048 | C | A | 1 | a0001c0002t0055 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1387C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1387 | chr17 | 6122048 | ||||||
chr17:6122152 | C | T | 23 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0021 others(20): Show |
68 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1491C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1491 | chr17 | 6122152 | ||||||
chr17:6122199 | C | A | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0021 others(28): Show |
77 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1538C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1538 | chr17 | 6122199 | ||||||
chr17:6122408 | T | C | 1 | a0001c0002t0057 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1747T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1747 | chr17 | 6122408 | ||||||
chr17:6122468 | G | A | 139 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(136): Show |
420 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(417): Show |
3_prime_UTR_variant | MODIFIER | c.*1807G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1807 | chr17 | 6122468 | ||||||
chr17:6122475 | A | G | 1 | a0001c0002t0051 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1814A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1814 | chr17 | 6122475 | ||||||
chr17:6122560 | C | T | 27 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(24): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1899C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1899 | chr17 | 6122560 | ||||||
chr17:6122590 | A | C | 29 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0028 others(26): Show |
139 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*1929A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1929 | chr17 | 6122590 | ||||||
chr17:6122593 | A | G | 1 | a0001c0004t0068 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1932A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1932 | chr17 | 6122593 | ||||||
chr17:6122622 | C | T | 26 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0028 others(23): Show |
136 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1961C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1961 | chr17 | 6122622 | ||||||
chr17:6122623 | G | A | 3 | a0001c0001t0069 a0001c0002t0032 a0001c0004t0032 |
3 | HG01975.hp1 NA18992.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1962G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1962 | chr17 | 6122623 | ||||||
chr17:6122650 | G | A | 1 | a0001c0001t0058 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1989G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 1989 | chr17 | 6122650 | ||||||
chr17:6122688 | G | A | 3 | a0001c0002t0054 a0001c0003t0076 a0001c0004t0073 |
3 | HG02572.hp2 HG02630.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2027G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2027 | chr17 | 6122688 | ||||||
chr17:6122706 | A | G | 1 | a0001c0001t0053 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2045A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2045 | chr17 | 6122706 | ||||||
chr17:6122849 | G | A | 2 | a0001c0001t0006 a0001c0002t0006 |
10 | HG00597.hp1 HG02015.hp1 HG02523.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2188G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2188 | chr17 | 6122849 | ||||||
chr17:6122888 | CTGAGTCA others(27): Show |
C | 1 | a0001c0001t0066 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2228_*2261delTGAG others(30): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2228 | chr17 | 6122888 | ||||||
chr17:6122972 | A | C | 5 | a0001c0001t0012 a0001c0001t0045 a0001c0001t0050 others(2): Show |
7 | HG01069.hp2 HG01109.hp1 HG02004.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2311A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2311 | chr17 | 6122972 | ||||||
chr17:6123008 | T | G | 4 | a0001c0002t0049 a0001c0002t0070 a0001c0003t0044 others(1): Show |
4 | HG01167.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2347T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2347 | chr17 | 6123008 | ||||||
chr17:6123013 | A | G | 3 | a0001c0001t0010 a0001c0002t0010 a0001c0004t0068 |
7 | NA18940.hp2 NA18943.hp2 NA18957.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2352A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2352 | chr17 | 6123013 | ||||||
chr17:6123014 | C | T | 2 | a0001c0001t0060 a0003c0005t0074 |
2 | HG03139.hp2 NA18991.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2353C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2353 | chr17 | 6123014 | ||||||
chr17:6123247 | A | G | 29 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0028 others(26): Show |
140 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*2586A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2586 | chr17 | 6123247 | ||||||
chr17:6123366 | A | G | 1 | a0001c0001t0048 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2705A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2705 | chr17 | 6123366 | ||||||
chr17:6123563 | A | G | 4 | a0001c0002t0049 a0001c0002t0070 a0001c0003t0044 others(1): Show |
4 | HG01167.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2902A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 2902 | chr17 | 6123563 | ||||||
chr17:6123699 | A | G | 1 | a0001c0002t0067 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3038A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 3038 | chr17 | 6123699 | ||||||
chr17:6123740 | T | C | 10 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0025 others(7): Show |
27 | HG00735.hp2 HG01515.hp1 HG01884.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3079T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 3079 | chr17 | 6123740 | ||||||
chr17:6123743 | G | A | 3 | a0001c0002t0054 a0001c0003t0076 a0001c0004t0073 |
3 | HG02572.hp2 HG02630.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3082G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 3082 | chr17 | 6123743 | ||||||
chr17:6123755 | A | G | 2 | a0001c0002t0013 a0001c0002t0042 |
6 | HG02965.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3094A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 3094 | chr17 | 6123755 | ||||||
chr17:6123827 | A | C | 2 | a0001c0001t0038 a0001c0001t0063 |
3 | NA18950.hp1 NA18960.hp2 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3166A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 3166 | chr17 | 6123827 | ||||||
chr17:6123893 | C | T | 1 | a0001c0002t0051 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3232C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 3232 | chr17 | 6123893 | ||||||
chr17:6124036 | A | G | 1 | a0001c0001t0033 | 2 | HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3375A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 3375 | chr17 | 6124036 | ||||||
chr17:6124098 | C | T | 1 | a0001c0001t0037 | 2 | HG00741.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3437C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 9/9 | 3437 | chr17 | 6124098 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:6070798 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-289+146C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6070798 | |||||||
chr17:6070872 | T | TG | 15 | a0001c0001t0001g0390 a0001c0001t0001g0393 a0001c0001t0001g0400 others(12): Show |
15 | HG00408.hp1 HG00597.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289+227dupG | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | 6070872 | ||||||
chr17:6070893 | C | T | 2 | a0001c0004t0073g0386 a0003c0005t0074g0387 |
2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-289+241C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6070893 | |||||||
chr17:6070923 | G | T | 5 | a0001c0001t0080g0382 a0001c0002t0025g0383 a0001c0002t0077g0381 others(2): Show |
5 | HG01243.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-289+271G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6070923 | |||||||
chr17:6071007 | G | T | 1 | a0001c0002t0018g0380 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-289+355G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6071007 | |||||||
chr17:6071043 | C | T | 1 | a0001c0002t0054g0379 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-289+391C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6071043 | |||||||
chr17:6071286 | G | A | 11 | a0001c0001t0003g0030 a0001c0002t0001g0032 a0001c0002t0001g0034 others(8): Show |
11 | HG00738.hp2 HG01081.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.-289+634G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6071286 | |||||||
chr17:6071411 | C | T | 3 | a0001c0002t0004g0377 a0001c0002t0081g0376 a0001c0003t0076g0378 |
3 | HG02572.hp2 HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-289+759C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6071411 | |||||||
chr17:6071494 | C | T | 1 | a0001c0002t0014g0375 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-289+842C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6071494 | |||||||
chr17:6071610 | T | G | 5 | a0001c0001t0035g0035 a0001c0002t0004g0389 a0001c0002t0015g0036 others(2): Show |
5 | HG02055.hp1 HG02886.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-289+958T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6071610 | |||||||
chr17:6071723 | A | G | 237 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(234): Show |
245 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.-289+1071A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6071723 | |||||||
chr17:6071980 | C | T | 231 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(228): Show |
239 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.-289+1328C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6071980 | |||||||
chr17:6072032 | G | T | 1 | a0002c0007t0023g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-289+1380G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6072032 | |||||||
chr17:6072157 | T | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0219 a0001c0001t0001g0221 others(80): Show |
88 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.-289+1505T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6072157 | |||||||
chr17:6072523 | G | A | 121 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(118): Show |
125 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-289+1871G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6072523 | |||||||
chr17:6072680 | G | C | 3 | a0001c0002t0008g0020 a0001c0002t0008g0246 a0001c0002t0008g0247 |
4 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-289+2028G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6072680 | |||||||
chr17:6072722 | T | C | 2 | a0001c0002t0001g0016 a0001c0002t0004g0182 |
3 | HG01256.hp1 HG01258.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-289+2070T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6072722 | |||||||
chr17:6072849 | A | G | 1 | a0001c0002t0004g0374 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-289+2197A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6072849 | |||||||
chr17:6072992 | C | T | 192 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(189): Show |
199 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.-289+2340C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6072992 | |||||||
chr17:6073030 | T | C | 3 | a0001c0001t0003g0249 a0001c0001t0050g0250 a0001c0002t0003g0248 |
3 | HG00733.hp2 HG01952.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-289+2378T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073030 | |||||||
chr17:6073031 | G | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
208 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.-289+2379G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073031 | |||||||
chr17:6073094 | A | T | 2 | a0001c0002t0001g0034 a0009c0019t0002g0033 |
2 | HG02300.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-289+2442A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073094 | |||||||
chr17:6073217 | C | T | 4 | a0001c0002t0007g0242 a0001c0002t0007g0244 a0001c0002t0023g0243 others(1): Show |
4 | HG02717.hp2 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-289+2565C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073217 | |||||||
chr17:6073253 | G | A | 1 | a0002c0007t0090g0184 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-289+2601G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073253 | |||||||
chr17:6073280 | T | A | 1 | a0001c0002t0004g0041 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-289+2628T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073280 | |||||||
chr17:6073291 | G | A | 1 | a0001c0002t0003g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-289+2639G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073291 | |||||||
chr17:6073315 | A | G | 400 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(397): Show |
416 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(413): Show |
intron_variant | MODIFIER | c.-289+2663A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073315 | |||||||
chr17:6073446 | A | T | 2 | a0001c0004t0073g0386 a0003c0005t0074g0387 |
2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-289+2794A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073446 | |||||||
chr17:6073540 | A | G | 2 | a0001c0002t0001g0032 a0001c0002t0002g0031 |
2 | HG01081.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-289+2888A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073540 | |||||||
chr17:6073546 | C | G | 1 | a0001c0001t0002g0241 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-289+2894C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073546 | |||||||
chr17:6073571 | G | A | 3 | a0001c0001t0003g0196 a0001c0002t0054g0379 a0001c0002t0070g0354 |
3 | HG00639.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-289+2919G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073571 | |||||||
chr17:6073624 | C | T | 1 | a0001c0001t0004g0341 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-289+2972C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073624 | |||||||
chr17:6073762 | G | C | 287 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(284): Show |
299 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.-289+3110G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6073762 | |||||||
chr17:6074082 | T | A | 4 | a0001c0002t0004g0377 a0001c0002t0077g0381 a0001c0002t0081g0376 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-289+3430T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6074082 | |||||||
chr17:6074240 | G | A | 2 | a0001c0004t0073g0386 a0003c0005t0074g0387 |
2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-289+3588G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6074240 | |||||||
chr17:6074293 | C | G | 1 | a0001c0002t0015g0174 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-289+3641C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6074293 | |||||||
chr17:6074303 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-289+3651C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6074303 | |||||||
chr17:6074432 | T | C | 8 | a0001c0001t0001g0361 a0001c0001t0002g0357 a0001c0001t0002g0362 others(5): Show |
8 | HG00423.hp2 HG02155.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.-289+3780T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6074432 | |||||||
chr17:6074695 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-289+4043C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6074695 | |||||||
chr17:6074763 | G | A | 2 | a0001c0004t0073g0386 a0003c0005t0074g0387 |
2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-289+4111G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6074763 | |||||||
chr17:6074983 | G | A | 1 | a0001c0001t0008g0251 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-289+4331G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6074983 | |||||||
chr17:6075025 | G | A | 4 | a0001c0002t0013g0165 a0001c0002t0017g0163 a0001c0004t0007g0164 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-289+4373G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075025 | |||||||
chr17:6075094 | T | A | 196 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(193): Show |
204 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.-289+4442T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075094 | |||||||
chr17:6075269 | T | A | 8 | a0001c0001t0001g0361 a0001c0001t0002g0357 a0001c0001t0002g0362 others(5): Show |
8 | HG00423.hp2 HG02155.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.-289+4617T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075269 | |||||||
chr17:6075343 | A | T | 1 | a0001c0002t0015g0174 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-289+4691A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075343 | |||||||
chr17:6075419 | C | T | 7 | a0001c0002t0014g0171 a0001c0002t0017g0015 a0001c0002t0031g0015 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-289+4767C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075419 | |||||||
chr17:6075444 | G | C | 1 | a0001c0001t0002g0364 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-289+4792G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075444 | |||||||
chr17:6075476 | ACCCATCA others(10): Show |
A | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-289+4825_-289+484 others(21): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075476 | |||||||
chr17:6075624 | C | G | 3 | a0001c0002t0054g0379 a0001c0002t0070g0354 a0002c0007t0003g0168 |
3 | HG02145.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-288-4747C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075624 | |||||||
chr17:6075656 | T | A | 8 | a0001c0001t0001g0361 a0001c0001t0002g0357 a0001c0001t0002g0362 others(5): Show |
8 | HG00423.hp2 HG02155.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.-288-4715T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075656 | |||||||
chr17:6075784 | T | A | 1 | a0001c0003t0044g0333 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-288-4587T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075784 | |||||||
chr17:6075840 | A | C | 13 | a0001c0001t0035g0035 a0001c0002t0004g0167 a0001c0002t0013g0165 others(10): Show |
13 | HG01109.hp2 HG01891.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-288-4531A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075840 | |||||||
chr17:6075879 | G | T | 1 | a0001c0001t0019g0150 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-288-4492G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075879 | |||||||
chr17:6075929 | C | CACGGACA others(1): Show |
36 | a0001c0001t0001g0361 a0001c0001t0002g0357 a0001c0001t0002g0362 others(33): Show |
36 | HG00423.hp2 HG01243.hp2 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.-288-4441_-288-443 others(12): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | 6075929 | ||||||
chr17:6075932 | G | A | 7 | a0001c0002t0026g0200 a0001c0002t0026g0204 a0001c0002t0026g0205 others(4): Show |
7 | HG01891.hp2 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-288-4439G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075932 | |||||||
chr17:6075982 | T | A | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-288-4389T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6075982 | |||||||
chr17:6076025 | T | C | 7 | a0001c0002t0004g0374 a0001c0002t0017g0179 a0001c0002t0049g0366 others(4): Show |
7 | HG01167.hp1 HG02055.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-288-4346T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076025 | |||||||
chr17:6076150 | C | T | 1 | a0001c0002t0001g0240 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-288-4221C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076150 | |||||||
chr17:6076218 | A | G | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-288-4153A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076218 | |||||||
chr17:6076219 | G | A | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-288-4152G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076219 | |||||||
chr17:6076336 | G | A | 3 | a0001c0001t0002g0151 a0001c0002t0002g0153 a0001c0002t0055g0152 |
3 | HG00438.hp1 NA19004.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-288-4035G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076336 | |||||||
chr17:6076403 | A | C | 45 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0001g0238 others(42): Show |
48 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.-288-3968A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076403 | |||||||
chr17:6076488 | C | T | 10 | a0001c0002t0014g0171 a0001c0002t0017g0015 a0001c0002t0031g0015 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-288-3883C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076488 | |||||||
chr17:6076501 | C | T | 1 | a0001c0001t0002g0331 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-288-3870C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076501 | |||||||
chr17:6076613 | T | G | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-288-3758T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076613 | |||||||
chr17:6076647 | G | T | 1 | a0001c0001t0001g0356 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-288-3724G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076647 | |||||||
chr17:6076713 | A | T | 94 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(91): Show |
98 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-288-3658A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076713 | |||||||
chr17:6076736 | C | T | 1 | a0001c0004t0004g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-288-3635C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076736 | |||||||
chr17:6076780 | C | T | 56 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0117 others(53): Show |
58 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-288-3591C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076780 | |||||||
chr17:6076792 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
203 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.-288-3579T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076792 | |||||||
chr17:6076794 | G | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(95): Show |
102 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-288-3577G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076794 | |||||||
chr17:6076901 | G | A | 3 | a0001c0002t0054g0379 a0001c0002t0070g0354 a0002c0007t0003g0168 |
3 | HG02145.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-288-3470G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076901 | |||||||
chr17:6076963 | C | T | 3 | a0001c0002t0054g0379 a0001c0002t0070g0354 a0002c0007t0003g0168 |
3 | HG02145.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-288-3408C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6076963 | |||||||
chr17:6077011 | A | C | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-288-3360A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077011 | |||||||
chr17:6077015 | T | C | 45 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0001g0238 others(42): Show |
48 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.-288-3356T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077015 | |||||||
chr17:6077088 | C | CT | 19 | a0001c0001t0001g0162 a0001c0001t0001g0329 a0001c0001t0002g0362 others(16): Show |
19 | HG01070.hp1 HG01109.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.-288-3264dupT | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | 6077088 | ||||||
chr17:6077088 | CT | C | 69 | a0001c0001t0001g0046 a0001c0001t0001g0219 a0001c0001t0001g0221 others(66): Show |
72 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-288-3264delT | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | 6077088 | ||||||
chr17:6077088 | CTT | C | 8 | a0001c0001t0069g0209 a0001c0002t0001g0213 a0001c0002t0002g0210 others(5): Show |
8 | HG00642.hp1 HG01099.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.-288-3265_-288-326 others(6): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | 6077088 | ||||||
chr17:6077162 | C | T | 1 | a0001c0001t0009g0401 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-288-3209C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077162 | |||||||
chr17:6077174 | C | T | 1 | a0002c0007t0090g0184 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-288-3197C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077174 | |||||||
chr17:6077332 | C | T | 1 | a0001c0003t0044g0333 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-288-3039C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077332 | |||||||
chr17:6077358 | A | ATC | 29 | a0001c0001t0001g0361 a0001c0001t0002g0357 a0001c0001t0002g0362 others(26): Show |
29 | HG00423.hp2 HG01167.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.-288-3012_-288-301 others(6): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | 6077358 | ||||||
chr17:6077585 | G | A | 1 | a0001c0002t0013g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-288-2786G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077585 | |||||||
chr17:6077655 | C | T | 3 | a0001c0002t0008g0020 a0001c0002t0008g0246 a0001c0002t0008g0247 |
4 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-288-2716C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077655 | |||||||
chr17:6077733 | T | C | 401 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(398): Show |
417 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(414): Show |
intron_variant | MODIFIER | c.-288-2638T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077733 | |||||||
chr17:6077762 | T | C | 8 | a0001c0001t0001g0361 a0001c0001t0002g0357 a0001c0001t0002g0362 others(5): Show |
8 | HG00423.hp2 HG02155.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.-288-2609T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077762 | |||||||
chr17:6077819 | C | A | 1 | a0001c0001t0001g0050 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-288-2552C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077819 | |||||||
chr17:6077823 | T | C | 1 | a0001c0003t0044g0333 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-288-2548T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077823 | |||||||
chr17:6077867 | C | T | 2 | a0001c0001t0003g0147 a0001c0002t0002g0328 |
2 | HG02040.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-288-2504C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077867 | |||||||
chr17:6077949 | C | T | 1 | a0001c0001t0001g0361 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-288-2422C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077949 | |||||||
chr17:6077996 | T | C | 1 | a0001c0002t0017g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-288-2375T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6077996 | |||||||
chr17:6078031 | C | T | 1 | a0001c0002t0013g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-288-2340C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078031 | |||||||
chr17:6078035 | G | C | 1 | a0001c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-288-2336G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078035 | |||||||
chr17:6078067 | A | G | 13 | a0001c0001t0001g0361 a0001c0001t0002g0357 a0001c0001t0002g0362 others(10): Show |
13 | HG00423.hp2 HG01243.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-288-2304A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078067 | |||||||
chr17:6078241 | T | C | 291 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(288): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.-288-2130T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078241 | |||||||
chr17:6078303 | G | A | 2 | a0002c0006t0015g0111 a0002c0006t0056g0110 |
2 | HG01070.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-288-2068G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078303 | |||||||
chr17:6078342 | G | C | 1 | a0001c0004t0073g0386 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-288-2029G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078342 | |||||||
chr17:6078351 | G | A | 3 | a0001c0002t0015g0174 a0002c0006t0015g0111 a0002c0006t0056g0110 |
3 | HG01070.hp1 HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-288-2020G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078351 | |||||||
chr17:6078530 | C | T | 1 | a0001c0003t0044g0333 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-288-1841C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078530 | |||||||
chr17:6078561 | G | GGT | 9 | a0001c0001t0001g0361 a0001c0001t0002g0357 a0001c0001t0002g0362 others(6): Show |
9 | HG00423.hp2 HG01261.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-288-1792_-288-179 others(6): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | 6078561 | ||||||
chr17:6078561 | GGTGT | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0052 |
3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-288-1794_-288-179 others(8): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | 6078561 | ||||||
chr17:6078563 | T | G | 1 | a0001c0001t0002g0268 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-288-1808T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078563 | |||||||
chr17:6078591 | C | T | 1 | a0001c0002t0004g0167 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-288-1780C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078591 | |||||||
chr17:6078678 | G | C | 8 | a0001c0001t0001g0361 a0001c0001t0002g0357 a0001c0001t0002g0362 others(5): Show |
8 | HG00423.hp2 HG02155.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.-288-1693G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078678 | |||||||
chr17:6078723 | C | A | 6 | a0001c0001t0035g0035 a0001c0002t0015g0036 a0001c0002t0015g0037 others(3): Show |
6 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-288-1648C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078723 | |||||||
chr17:6078729 | G | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(82): Show |
89 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-288-1642G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078729 | |||||||
chr17:6078741 | C | T | 1 | a0001c0002t0072g0262 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-288-1630C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078741 | |||||||
chr17:6078843 | G | T | 5 | a0001c0001t0007g0044 a0001c0002t0051g0186 a0001c0003t0035g0245 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-288-1528G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078843 | |||||||
chr17:6078961 | T | A | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-288-1410T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078961 | |||||||
chr17:6078973 | G | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(214): Show |
226 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(223): Show |
intron_variant | MODIFIER | c.-288-1398G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6078973 | |||||||
chr17:6079049 | C | T | 1 | a0001c0003t0035g0245 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-288-1322C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079049 | |||||||
chr17:6079097 | G | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
236 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.-288-1274G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079097 | |||||||
chr17:6079181 | A | G | 9 | a0001c0001t0007g0044 a0001c0001t0035g0035 a0001c0002t0004g0167 others(6): Show |
9 | HG02559.hp2 HG02615.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-288-1190A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079181 | |||||||
chr17:6079263 | C | CG | 29 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0102 others(26): Show |
30 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-288-1102dupG | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr17 | 6079263 | ||||||
chr17:6079288 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-288-1083C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079288 | |||||||
chr17:6079307 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-288-1064G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079307 | |||||||
chr17:6079345 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0003g0010 |
3 | HG01069.hp1 HG01071.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-288-1026T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079345 | |||||||
chr17:6079431 | C | T | 6 | a0001c0002t0026g0200 a0001c0002t0026g0205 a0001c0002t0091g0201 others(3): Show |
6 | HG01891.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-288-940C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079431 | |||||||
chr17:6079446 | G | A | 1 | a0001c0001t0021g0257 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-288-925G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079446 | |||||||
chr17:6079467 | G | A | 8 | a0001c0001t0035g0035 a0001c0002t0015g0036 a0001c0002t0015g0037 others(5): Show |
8 | HG02572.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-288-904G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079467 | |||||||
chr17:6079557 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-288-814C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079557 | |||||||
chr17:6079614 | G | T | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-288-757G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079614 | |||||||
chr17:6079667 | C | T | 405 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(402): Show |
421 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(418): Show |
intron_variant | MODIFIER | c.-288-704C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079667 | |||||||
chr17:6079763 | A | G | 5 | a0001c0002t0016g0332 a0001c0002t0016g0358 a0001c0002t0016g0360 others(2): Show |
5 | HG00423.hp2 NA18940.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.-288-608A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079763 | |||||||
chr17:6079808 | C | T | 13 | a0001c0001t0007g0044 a0001c0001t0080g0382 a0001c0002t0004g0167 others(10): Show |
13 | HG01243.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-288-563C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079808 | |||||||
chr17:6079813 | C | T | 3 | a0001c0002t0075g0181 a0001c0002t0081g0376 a0001c0003t0076g0378 |
3 | HG02572.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-288-558C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079813 | |||||||
chr17:6079949 | G | A | 11 | a0001c0001t0080g0382 a0001c0002t0004g0167 a0001c0002t0014g0171 others(8): Show |
11 | HG01243.hp2 HG01884.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-288-422G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6079949 | |||||||
chr17:6080066 | T | C | 3 | a0001c0002t0017g0179 a0001c0002t0022g0254 a0001c0002t0022g0255 |
3 | HG02572.hp1 HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-288-305T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6080066 | |||||||
chr17:6080075 | T | C | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-288-296T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6080075 | |||||||
chr17:6080169 | G | A | 1 | a0001c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-288-202G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6080169 | |||||||
chr17:6080220 | A | G | 26 | a0001c0001t0007g0044 a0001c0001t0080g0382 a0001c0002t0004g0041 others(23): Show |
26 | HG00423.hp2 HG01243.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-288-151A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 1/8 | chr17 | 6080220 | |||||||
chr17:6081090 | G | A | 1 | a0001c0001t0002g0268 | 1 | HG02056.hp1 | splice_region_variant&intron_variant | LOW | c.427+5G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081090 | |||||||
chr17:6081125 | C | G | 3 | a0001c0002t0026g0205 a0003c0005t0020g0343 a0003c0005t0020g0345 |
3 | HG02486.hp2 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.427+40C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081125 | |||||||
chr17:6081131 | A | G | 5 | a0001c0002t0016g0332 a0001c0002t0016g0358 a0001c0002t0016g0360 others(2): Show |
5 | HG00423.hp2 NA18940.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.427+46A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081131 | |||||||
chr17:6081321 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0003g0012 a0001c0001t0005g0017 |
5 | HG01070.hp2 HG01071.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+236G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081321 | |||||||
chr17:6081325 | C | T | 1 | a0001c0001t0006g0273 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.427+240C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081325 | |||||||
chr17:6081346 | A | G | 27 | a0001c0001t0007g0044 a0001c0001t0080g0382 a0001c0002t0004g0041 others(24): Show |
27 | HG00423.hp2 HG01243.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.427+261A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081346 | |||||||
chr17:6081436 | C | T | 1 | a0001c0004t0032g0371 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.427+351C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081436 | |||||||
chr17:6081567 | C | T | 6 | a0001c0002t0004g0374 a0001c0002t0015g0174 a0001c0002t0049g0366 others(3): Show |
6 | HG01167.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.427+482C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081567 | |||||||
chr17:6081603 | C | G | 2 | a0005c0021t0004g0154 a0005c0022t0020g0155 |
2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.427+518C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081603 | |||||||
chr17:6081618 | C | A | 18 | a0001c0001t0007g0044 a0001c0001t0080g0382 a0001c0002t0004g0041 others(15): Show |
18 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.427+533C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081618 | |||||||
chr17:6081619 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0003g0012 a0001c0001t0005g0017 |
5 | HG01070.hp2 HG01071.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+534C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081619 | |||||||
chr17:6081652 | C | T | 2 | a0001c0002t0072g0262 a0003c0005t0074g0387 |
2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.427+567C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081652 | |||||||
chr17:6081677 | C | G | 25 | a0001c0001t0001g0046 a0001c0001t0001g0087 a0001c0001t0012g0088 others(22): Show |
26 | HG01884.hp1 HG02129.hp2 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.427+592C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081677 | |||||||
chr17:6081706 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.427+621A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081706 | |||||||
chr17:6081713 | G | A | 7 | a0001c0002t0016g0332 a0001c0002t0016g0358 a0001c0002t0016g0360 others(4): Show |
7 | HG00423.hp2 HG01243.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+628G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081713 | |||||||
chr17:6081713 | GA | G | 7 | a0001c0001t0001g0272 a0001c0002t0001g0092 a0001c0002t0001g0350 others(4): Show |
7 | HG02129.hp2 HG02155.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.427+640delA | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6081713 | ||||||
chr17:6081714 | A | G | 7 | a0001c0002t0016g0332 a0001c0002t0016g0358 a0001c0002t0016g0360 others(4): Show |
7 | HG00423.hp2 HG01243.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+629A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081714 | |||||||
chr17:6081733 | T | C | 8 | a0001c0002t0016g0332 a0001c0002t0016g0358 a0001c0002t0016g0360 others(5): Show |
8 | HG00423.hp2 HG01243.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.427+648T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081733 | |||||||
chr17:6081824 | T | C | 2 | a0001c0002t0054g0379 a0002c0007t0003g0168 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.427+739T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081824 | |||||||
chr17:6081827 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.427+742G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081827 | |||||||
chr17:6081882 | A | G | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | NA18988.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.427+797A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081882 | |||||||
chr17:6081959 | C | T | 1 | a0001c0001t0002g0103 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.427+874C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081959 | |||||||
chr17:6081989 | G | T | 10 | a0001c0001t0001g0261 a0001c0001t0003g0249 a0001c0001t0050g0250 others(7): Show |
10 | HG00423.hp2 HG00733.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.427+904G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6081989 | |||||||
chr17:6082018 | T | C | 396 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(393): Show |
411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.427+933T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082018 | |||||||
chr17:6082060 | A | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.427+975A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082060 | |||||||
chr17:6082080 | A | C | 74 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0001g0238 others(71): Show |
77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.427+995A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082080 | |||||||
chr17:6082119 | G | A | 2 | a0005c0021t0004g0154 a0005c0022t0020g0155 |
2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.427+1034G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082119 | |||||||
chr17:6082159 | A | G | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.427+1074A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082159 | |||||||
chr17:6082160 | G | C | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.427+1075G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082160 | |||||||
chr17:6082170 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0321 |
2 | NA18975.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.427+1085A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082170 | |||||||
chr17:6082180 | A | G | 62 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0001g0238 others(59): Show |
65 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.427+1095A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082180 | |||||||
chr17:6082186 | A | G | 63 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0001g0238 others(60): Show |
67 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.427+1101A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082186 | |||||||
chr17:6082242 | G | A | 1 | a0001c0003t0007g0326 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.427+1157G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082242 | |||||||
chr17:6082244 | G | A | 1 | a0001c0013t0004g0217 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.427+1159G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082244 | |||||||
chr17:6082288 | G | A | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.427+1203G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082288 | |||||||
chr17:6082292 | C | T | 2 | a0001c0001t0001g0261 a0001c0004t0073g0386 |
2 | HG01099.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.427+1207C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082292 | |||||||
chr17:6082436 | C | G | 7 | a0001c0001t0007g0044 a0001c0001t0007g0320 a0001c0002t0004g0167 others(4): Show |
7 | HG01243.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.427+1351C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082436 | |||||||
chr17:6082506 | T | C | 9 | a0001c0001t0007g0044 a0001c0002t0075g0181 a0001c0004t0004g0172 others(6): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.427+1421T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082506 | |||||||
chr17:6082715 | A | C | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.427+1630A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082715 | |||||||
chr17:6082721 | G | A | 7 | a0001c0002t0016g0332 a0001c0002t0016g0358 a0001c0002t0016g0360 others(4): Show |
7 | HG00423.hp2 HG02074.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.427+1636G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082721 | |||||||
chr17:6082812 | C | G | 1 | a0001c0002t0049g0366 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.427+1727C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082812 | |||||||
chr17:6082821 | G | A | 7 | a0003c0005t0014g0193 a0003c0005t0020g0343 a0003c0005t0020g0345 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+1736G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082821 | |||||||
chr17:6082870 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0003g0143 a0001c0009t0001g0394 |
3 | HG01261.hp2 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.427+1785C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6082870 | |||||||
chr17:6083021 | G | A | 1 | a0001c0003t0014g0256 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.427+1936G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083021 | |||||||
chr17:6083127 | G | A | 6 | a0001c0002t0004g0389 a0001c0002t0017g0015 a0001c0002t0020g0192 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+2042G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083127 | |||||||
chr17:6083172 | C | T | 23 | a0001c0001t0001g0014 a0001c0001t0006g0014 a0001c0002t0001g0141 others(20): Show |
23 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.427+2087C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083172 | |||||||
chr17:6083176 | A | C | 4 | a0001c0002t0015g0036 a0001c0002t0015g0037 a0001c0002t0025g0352 others(1): Show |
4 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.427+2091A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083176 | |||||||
chr17:6083347 | G | A | 2 | a0001c0002t0025g0383 a0001c0002t0078g0384 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.427+2262G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083347 | |||||||
chr17:6083373 | C | T | 1 | a0001c0001t0007g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.427+2288C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083373 | |||||||
chr17:6083396 | T | C | 2 | a0001c0002t0054g0379 a0002c0007t0003g0168 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.427+2311T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083396 | |||||||
chr17:6083445 | G | A | 3 | a0001c0001t0001g0261 a0001c0001t0003g0249 a0001c0001t0050g0250 |
3 | HG00733.hp2 HG01099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.427+2360G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083445 | |||||||
chr17:6083521 | A | G | 1 | a0001c0001t0004g0341 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.427+2436A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083521 | |||||||
chr17:6083592 | A | C | 1 | a0001c0002t0010g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.427+2507A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083592 | |||||||
chr17:6083600 | G | A | 1 | a0002c0007t0023g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.427+2515G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083600 | |||||||
chr17:6083661 | T | C | 1 | a0001c0002t0017g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.427+2576T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083661 | |||||||
chr17:6083693 | C | T | 1 | a0001c0002t0004g0316 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.427+2608C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083693 | |||||||
chr17:6083704 | A | G | 98 | a0001c0001t0001g0014 a0001c0001t0001g0221 a0001c0001t0001g0238 others(95): Show |
101 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.427+2619A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083704 | |||||||
chr17:6083727 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.427+2642C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083727 | |||||||
chr17:6083735 | C | T | 3 | a0001c0003t0031g0206 a0001c0003t0092g0202 a0002c0007t0090g0184 |
3 | HG02647.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.427+2650C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083735 | |||||||
chr17:6083748 | C | T | 1 | a0001c0002t0002g0090 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.427+2663C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083748 | |||||||
chr17:6083788 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(233): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.427+2703A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083788 | |||||||
chr17:6083796 | A | G | 2 | a0001c0002t0054g0379 a0002c0007t0003g0168 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.427+2711A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083796 | |||||||
chr17:6083801 | A | G | 10 | a0001c0001t0048g0349 a0001c0002t0052g0169 a0003c0005t0014g0193 others(7): Show |
10 | HG02257.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.427+2716A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6083801 | |||||||
chr17:6084030 | T | C | 341 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(338): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.427+2945T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084030 | |||||||
chr17:6084042 | G | A | 2 | a0001c0002t0018g0214 a0001c0003t0076g0378 |
2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.427+2957G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084042 | |||||||
chr17:6084335 | C | T | 2 | a0001c0002t0026g0204 a0001c0002t0026g0205 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.427+3250C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084335 | |||||||
chr17:6084373 | A | G | 2 | a0001c0002t0054g0379 a0002c0007t0003g0168 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.427+3288A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084373 | |||||||
chr17:6084424 | C | G | 1 | a0001c0001t0003g0030 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.427+3339C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084424 | |||||||
chr17:6084501 | G | T | 4 | a0001c0002t0015g0036 a0001c0002t0015g0037 a0001c0002t0025g0352 others(1): Show |
4 | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.427+3416G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084501 | |||||||
chr17:6084528 | C | T | 1 | a0001c0002t0015g0037 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.427+3443C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084528 | |||||||
chr17:6084695 | G | A | 3 | a0001c0002t0018g0214 a0001c0002t0029g0190 a0001c0003t0076g0378 |
3 | HG02280.hp2 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.428-3295G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084695 | |||||||
chr17:6084698 | G | A | 2 | a0001c0002t0008g0020 a0001c0002t0008g0246 |
3 | HG01074.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.428-3292G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084698 | |||||||
chr17:6084711 | C | T | 6 | a0001c0002t0004g0389 a0001c0002t0017g0015 a0001c0002t0020g0192 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-3279C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084711 | |||||||
chr17:6084800 | G | A | 6 | a0001c0002t0004g0389 a0001c0002t0017g0015 a0001c0002t0020g0192 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-3190G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084800 | |||||||
chr17:6084808 | G | A | 342 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(339): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.428-3182G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084808 | |||||||
chr17:6084859 | C | T | 18 | a0001c0001t0001g0014 a0001c0001t0006g0014 a0001c0002t0001g0141 others(15): Show |
18 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.428-3131C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084859 | |||||||
chr17:6084911 | C | T | 1 | a0001c0004t0004g0172 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.428-3079C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084911 | |||||||
chr17:6084933 | G | A | 1 | a0001c0002t0015g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.428-3057G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084933 | |||||||
chr17:6084944 | C | T | 1 | a0001c0001t0006g0314 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.428-3046C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084944 | |||||||
chr17:6084948 | G | A | 3 | a0001c0001t0001g0261 a0001c0001t0003g0249 a0001c0001t0050g0250 |
3 | HG00733.hp2 HG01099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.428-3042G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084948 | |||||||
chr17:6084967 | G | A | 1 | a0001c0002t0002g0090 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.428-3023G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084967 | |||||||
chr17:6084978 | C | T | 13 | a0001c0002t0004g0377 a0001c0002t0004g0389 a0001c0002t0007g0244 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.428-3012C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084978 | |||||||
chr17:6084979 | G | A | 1 | a0002c0007t0023g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.428-3011G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6084979 | |||||||
chr17:6085000 | A | G | 41 | a0001c0001t0001g0014 a0001c0001t0006g0014 a0001c0002t0001g0141 others(38): Show |
42 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.428-2990A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085000 | |||||||
chr17:6085115 | T | A | 40 | a0001c0001t0001g0014 a0001c0001t0006g0014 a0001c0002t0001g0141 others(37): Show |
41 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.428-2875T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085115 | |||||||
chr17:6085210 | A | T | 3 | a0001c0002t0017g0163 a0001c0002t0049g0366 a0001c0002t0057g0338 |
3 | HG01167.hp1 HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.428-2780A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085210 | |||||||
chr17:6085352 | T | C | 43 | a0001c0001t0001g0221 a0001c0001t0003g0196 a0001c0001t0003g0397 others(40): Show |
46 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.428-2638T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085352 | |||||||
chr17:6085426 | ACC | A | 17 | a0001c0002t0004g0389 a0001c0002t0007g0185 a0001c0002t0013g0009 others(14): Show |
18 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.428-2563_428-2562d others(4): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085426 | |||||||
chr17:6085514 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.428-2476C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085514 | |||||||
chr17:6085517 | C | T | 18 | a0001c0001t0001g0014 a0001c0001t0006g0014 a0001c0002t0001g0141 others(15): Show |
18 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.428-2473C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085517 | |||||||
chr17:6085527 | C | G | 337 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(334): Show |
352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.428-2463C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085527 | |||||||
chr17:6085672 | G | T | 14 | a0001c0002t0007g0185 a0001c0002t0013g0009 a0001c0002t0013g0049 others(11): Show |
15 | HG01243.hp2 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.428-2318G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085672 | |||||||
chr17:6085674 | G | A | 64 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0096 others(61): Show |
66 | HG00544.hp1 HG00558.hp2 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.428-2316G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085674 | |||||||
chr17:6085726 | T | C | 1 | a0001c0002t0054g0379 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.428-2264T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085726 | |||||||
chr17:6085777 | C | A | 1 | a0001c0001t0001g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.428-2213C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085777 | |||||||
chr17:6085850 | C | T | 1 | a0001c0002t0070g0354 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.428-2140C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085850 | |||||||
chr17:6085973 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.428-2017G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6085973 | |||||||
chr17:6086047 | C | A | 8 | a0003c0005t0014g0193 a0003c0005t0020g0343 a0003c0005t0020g0345 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.428-1943C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086047 | |||||||
chr17:6086119 | C | T | 8 | a0003c0005t0014g0193 a0003c0005t0020g0343 a0003c0005t0020g0345 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.428-1871C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086119 | |||||||
chr17:6086136 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
191 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.428-1854T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086136 | |||||||
chr17:6086205 | C | T | 217 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.428-1785C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086205 | |||||||
chr17:6086214 | T | C | 1 | a0001c0002t0017g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.428-1776T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086214 | |||||||
chr17:6086249 | T | C | 18 | a0001c0001t0001g0014 a0001c0001t0006g0014 a0001c0002t0001g0141 others(15): Show |
18 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.428-1741T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086249 | |||||||
chr17:6086249 | T | TATATATA others(6): Show |
1 | a0001c0003t0017g0365 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.428-1741_428-1740i others(15): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086249 | |||||||
chr17:6086249 | T | TTATATAT others(1): Show |
6 | a0001c0002t0013g0009 a0001c0002t0013g0049 a0001c0002t0013g0091 others(3): Show |
7 | HG02622.hp2 HG02965.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-1741_428-1740i others(10): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086249 | |||||||
chr17:6086249 | T | TTATATAT others(3): Show |
1 | a0001c0002t0075g0181 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.428-1741_428-1740i others(12): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086249 | |||||||
chr17:6086249 | T | TTATATAT others(5): Show |
3 | a0001c0002t0015g0174 a0001c0002t0025g0383 a0001c0002t0078g0384 |
3 | HG01243.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.428-1741_428-1740i others(14): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086249 | |||||||
chr17:6086249 | T | TTATATAT others(11): Show |
1 | a0001c0002t0029g0190 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.428-1741_428-1740i others(20): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086249 | |||||||
chr17:6086249 | T | TTATATAT others(13): Show |
1 | a0001c0002t0018g0214 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.428-1741_428-1740i others(22): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086249 | |||||||
chr17:6086249 | T | TTATATAT others(19): Show |
1 | a0001c0003t0004g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.428-1741_428-1740i others(28): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086249 | |||||||
chr17:6086249 | T | TTATATAT others(25): Show |
1 | a0001c0003t0004g0194 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.428-1741_428-1740i others(34): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086249 | |||||||
chr17:6086250 | C | CAT | 15 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0261 others(12): Show |
16 | HG00733.hp2 HG00738.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.428-1716_428-1715d others(4): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATAT | 60 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0069 others(57): Show |
63 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.428-1718_428-1715d others(6): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATAT | 13 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0400 others(10): Show |
13 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.428-1720_428-1715d others(8): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(3): Show |
3 | a0001c0001t0001g0081 a0001c0003t0044g0333 a0002c0007t0003g0168 |
3 | HG02145.hp1 HG03453.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.428-1724_428-1715d others(12): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(5): Show |
2 | a0001c0001t0002g0269 a0001c0001t0003g0313 |
2 | HG00609.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.428-1726_428-1715d others(14): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(23): Show |
1 | a0001c0002t0070g0354 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.428-1727_428-1726i others(32): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(9): Show |
7 | a0001c0001t0003g0147 a0001c0001t0008g0286 a0001c0001t0088g0282 others(4): Show |
7 | HG01081.hp2 HG01261.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-1730_428-1715d others(18): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(11): Show |
6 | a0001c0001t0001g0272 a0001c0001t0011g0134 a0001c0002t0005g0139 others(3): Show |
6 | HG02300.hp1 HG02300.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-1732_428-1715d others(20): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(13): Show |
16 | a0001c0001t0001g0083 a0001c0001t0001g0119 a0001c0001t0002g0118 others(13): Show |
16 | HG00558.hp2 HG01109.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.428-1734_428-1715d others(22): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(15): Show |
18 | a0001c0001t0001g0156 a0001c0001t0001g0285 a0001c0001t0002g0124 others(15): Show |
18 | HG00099.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.428-1736_428-1715d others(24): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(17): Show |
18 | a0001c0001t0001g0117 a0001c0001t0001g0125 a0001c0001t0001g0356 others(15): Show |
19 | HG00323.hp1 HG00544.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.428-1738_428-1715d others(26): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(19): Show |
13 | a0001c0001t0001g0290 a0001c0001t0002g0095 a0001c0001t0002g0126 others(10): Show |
14 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.428-1715_428-1714i others(28): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(21): Show |
7 | a0001c0001t0001g0096 a0001c0001t0001g0128 a0001c0001t0002g0082 others(4): Show |
7 | HG02109.hp2 HG02735.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-1715_428-1714i others(30): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(23): Show |
5 | a0001c0001t0002g0129 a0001c0002t0052g0169 a0001c0002t0085g0284 others(2): Show |
5 | HG01891.hp1 HG02129.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-1715_428-1714i others(32): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(25): Show |
9 | a0001c0001t0001g0370 a0001c0001t0002g0130 a0001c0001t0002g0357 others(6): Show |
9 | HG02132.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.428-1715_428-1714i others(34): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(34): Show |
1 | a0001c0001t0006g0273 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.428-1715_428-1714i others(43): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(27): Show |
6 | a0001c0001t0001g0050 a0001c0001t0010g0135 a0001c0001t0019g0136 others(3): Show |
6 | HG02622.hp1 HG02647.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-1715_428-1714i others(36): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(29): Show |
3 | a0001c0001t0005g0292 a0001c0002t0001g0016 a0004c0010t0040g0043 |
4 | HG01256.hp1 HG01258.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-1715_428-1714i others(38): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | CATATATA others(31): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0321 a0001c0002t0001g0232 |
3 | NA19012.hp1 NA19081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.428-1715_428-1714i others(40): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | C | T | 34 | a0001c0001t0001g0014 a0001c0001t0006g0014 a0001c0002t0001g0141 others(31): Show |
35 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.428-1740C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086250 | |||||||
chr17:6086250 | CAT | C | 6 | a0001c0002t0004g0389 a0001c0002t0017g0015 a0001c0002t0020g0192 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-1716_428-1715d others(4): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086250 | CATATATA others(5): Show |
C | 22 | a0001c0001t0001g0221 a0001c0001t0003g0196 a0001c0001t0003g0397 others(19): Show |
24 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.428-1726_428-1715d others(14): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086250 | ||||||
chr17:6086251 | A | T | 18 | a0001c0001t0001g0014 a0001c0001t0006g0014 a0001c0002t0001g0141 others(15): Show |
18 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.428-1739A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086251 | |||||||
chr17:6086252 | T | A | 18 | a0001c0001t0001g0014 a0001c0001t0006g0014 a0001c0002t0001g0141 others(15): Show |
18 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.428-1738T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086252 | |||||||
chr17:6086274 | T | TATATATA others(17): Show |
1 | a0001c0013t0004g0217 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.428-1715_428-1714i others(26): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr17 | 6086274 | ||||||
chr17:6086276 | C | G | 4 | a0001c0002t0017g0163 a0001c0002t0049g0366 a0001c0002t0057g0338 others(1): Show |
4 | HG01167.hp1 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-1714C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086276 | |||||||
chr17:6086321 | A | G | 1 | a0001c0003t0089g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.428-1669A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086321 | |||||||
chr17:6086332 | T | G | 1 | a0001c0001t0002g0066 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.428-1658T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086332 | |||||||
chr17:6086758 | C | T | 41 | a0001c0001t0001g0221 a0001c0001t0003g0196 a0001c0001t0003g0397 others(38): Show |
44 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.428-1232C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086758 | |||||||
chr17:6086759 | A | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.428-1231A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086759 | |||||||
chr17:6086824 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(233): Show |
246 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.428-1166T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086824 | |||||||
chr17:6086834 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
220 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.428-1156G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086834 | |||||||
chr17:6086838 | C | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
186 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.428-1152C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086838 | |||||||
chr17:6086904 | G | T | 2 | a0001c0001t0002g0124 a0001c0001t0021g0148 |
2 | NA19005.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.428-1086G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086904 | |||||||
chr17:6086969 | C | T | 2 | a0001c0002t0054g0379 a0001c0002t0070g0354 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.428-1021C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6086969 | |||||||
chr17:6087068 | T | C | 1 | a0001c0002t0015g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.428-922T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6087068 | |||||||
chr17:6087079 | G | A | 1 | a0001c0002t0017g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.428-911G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6087079 | |||||||
chr17:6087181 | T | C | 1 | a0001c0001t0065g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.428-809T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6087181 | |||||||
chr17:6087183 | A | G | 293 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.428-807A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6087183 | |||||||
chr17:6087187 | C | T | 1 | a0001c0001t0037g0348 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.428-803C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6087187 | |||||||
chr17:6087262 | A | G | 6 | a0001c0002t0004g0389 a0001c0002t0017g0015 a0001c0002t0020g0192 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-728A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6087262 | |||||||
chr17:6087470 | A | G | 1 | a0001c0003t0001g0236 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.428-520A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6087470 | |||||||
chr17:6087574 | G | A | 14 | a0001c0002t0007g0185 a0001c0002t0013g0009 a0001c0002t0013g0049 others(11): Show |
15 | HG01243.hp2 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.428-416G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6087574 | |||||||
chr17:6087752 | G | A | 1 | a0001c0004t0002g0337 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.428-238G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 2/8 | chr17 | 6087752 | |||||||
chr17:6088286 | G | C | 8 | a0003c0005t0014g0193 a0003c0005t0020g0343 a0003c0005t0020g0345 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.542+182G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6088286 | |||||||
chr17:6088326 | G | A | 2 | a0001c0002t0015g0054 a0001c0003t0007g0326 |
2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.542+222G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6088326 | |||||||
chr17:6088399 | C | T | 1 | a0003c0005t0079g0385 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.542+295C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6088399 | |||||||
chr17:6088496 | A | G | 8 | a0003c0005t0014g0193 a0003c0005t0020g0343 a0003c0005t0020g0345 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.542+392A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6088496 | |||||||
chr17:6088696 | GCA | G | 315 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(312): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.542+611_542+612del others(2): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr17 | 6088696 | ||||||
chr17:6088786 | C | CT | 236 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
246 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.542+696dupT | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr17 | 6088786 | ||||||
chr17:6088786 | C | CTT | 52 | a0001c0001t0001g0161 a0001c0001t0002g0391 a0001c0001t0003g0048 others(49): Show |
55 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.542+695_542+696dup others(2): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr17 | 6088786 | ||||||
chr17:6088786 | C | CTTT | 19 | a0001c0002t0004g0377 a0001c0002t0007g0185 a0001c0002t0013g0009 others(16): Show |
20 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.542+694_542+696dup others(3): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr17 | 6088786 | ||||||
chr17:6088846 | G | T | 19 | a0001c0002t0004g0377 a0001c0002t0007g0185 a0001c0002t0013g0009 others(16): Show |
20 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.542+742G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6088846 | |||||||
chr17:6088927 | C | T | 1 | a0001c0001t0003g0397 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.542+823C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6088927 | |||||||
chr17:6088928 | G | A | 1 | a0001c0002t0004g0342 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.542+824G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6088928 | |||||||
chr17:6088971 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0011g0134 a0001c0001t0019g0136 |
3 | NA18943.hp1 NA19007.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.542+867A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6088971 | |||||||
chr17:6088984 | G | A | 2 | a0001c0002t0001g0208 a0001c0002t0001g0317 |
2 | HG00609.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.542+880G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6088984 | |||||||
chr17:6089023 | C | G | 19 | a0001c0002t0004g0377 a0001c0002t0007g0185 a0001c0002t0013g0009 others(16): Show |
20 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.542+919C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089023 | |||||||
chr17:6089028 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0003g0196 a0001c0001t0003g0397 others(1): Show |
4 | HG00639.hp1 HG01175.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+924C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089028 | |||||||
chr17:6089029 | G | A | 2 | a0001c0002t0001g0388 a0001c0003t0046g0029 |
2 | HG00738.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.542+925G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089029 | |||||||
chr17:6089084 | A | G | 1 | a0001c0001t0002g0095 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.542+980A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089084 | |||||||
chr17:6089108 | T | C | 2 | a0001c0001t0007g0320 a0001c0004t0073g0386 |
2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.542+1004T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089108 | |||||||
chr17:6089154 | T | C | 342 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(339): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.542+1050T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089154 | |||||||
chr17:6089155 | G | A | 1 | a0001c0001t0030g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.542+1051G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089155 | |||||||
chr17:6089258 | C | T | 1 | a0001c0002t0004g0167 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.543-1063C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089258 | |||||||
chr17:6089333 | G | A | 1 | a0001c0004t0004g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.543-988G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089333 | |||||||
chr17:6089391 | A | C | 1 | a0001c0001t0003g0143 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.543-930A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089391 | |||||||
chr17:6089472 | C | T | 12 | a0001c0001t0001g0080 a0001c0001t0001g0272 a0001c0001t0002g0076 others(9): Show |
12 | HG01943.hp1 NA18946.hp2 NA18963.hp2 others(9): Show |
intron_variant | MODIFIER | c.543-849C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089472 | |||||||
chr17:6089788 | G | A | 17 | a0001c0002t0004g0377 a0001c0002t0007g0185 a0001c0002t0013g0009 others(14): Show |
18 | HG01243.hp2 HG01884.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.543-533G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089788 | |||||||
chr17:6089848 | G | A | 1 | a0001c0002t0015g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.543-473G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089848 | |||||||
chr17:6089854 | C | A | 1 | a0001c0003t0007g0326 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.543-467C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089854 | |||||||
chr17:6089995 | G | A | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.543-326G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6089995 | |||||||
chr17:6090067 | G | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.543-254G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6090067 | |||||||
chr17:6090077 | C | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.543-244C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6090077 | |||||||
chr17:6090163 | G | A | 55 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0083 others(52): Show |
57 | HG00544.hp1 HG00558.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.543-158G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6090163 | |||||||
chr17:6090210 | CAA | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.543-102_543-101del others(2): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr17 | 6090210 | ||||||
chr17:6090218 | A | G | 11 | a0001c0002t0007g0185 a0001c0002t0013g0009 a0001c0002t0013g0049 others(8): Show |
12 | HG01243.hp2 HG02486.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.543-103A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6090218 | |||||||
chr17:6090262 | T | C | 1 | a0001c0001t0038g0068 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.543-59T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 3/8 | chr17 | 6090262 | |||||||
chr17:6090798 | C | T | 1 | a0001c0003t0007g0326 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.727+293C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6090798 | |||||||
chr17:6090826 | C | T | 6 | a0001c0002t0017g0015 a0001c0002t0020g0192 a0001c0002t0023g0243 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.727+321C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6090826 | |||||||
chr17:6091016 | G | A | 1 | a0001c0002t0002g0340 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.727+511G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6091016 | |||||||
chr17:6091073 | T | C | 8 | a0003c0005t0014g0193 a0003c0005t0020g0343 a0003c0005t0020g0345 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.727+568T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6091073 | |||||||
chr17:6091214 | G | A | 325 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(322): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.727+709G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6091214 | |||||||
chr17:6091634 | T | C | 11 | a0001c0002t0004g0191 a0001c0002t0004g0389 a0001c0002t0022g0047 others(8): Show |
11 | HG01106.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.727+1129T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6091634 | |||||||
chr17:6091790 | G | C | 1 | a0001c0002t0018g0214 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.727+1285G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6091790 | |||||||
chr17:6091893 | A | C | 1 | a0001c0002t0077g0381 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.727+1388A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6091893 | |||||||
chr17:6091900 | T | C | 1 | a0002c0006t0056g0110 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.727+1395T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6091900 | |||||||
chr17:6091928 | G | A | 1 | a0001c0003t0031g0206 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.727+1423G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6091928 | |||||||
chr17:6091960 | G | T | 1 | a0001c0002t0001g0351 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.727+1455G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6091960 | |||||||
chr17:6091962 | C | T | 1 | a0001c0002t0001g0388 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.727+1457C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6091962 | |||||||
chr17:6091976 | GA | G | 2 | a0001c0001t0001g0022 a0001c0001t0003g0147 |
3 | HG03490.hp2 HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.727+1475delA | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6091976 | ||||||
chr17:6092038 | T | C | 1 | a0001c0001t0012g0088 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.727+1533T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6092038 | |||||||
chr17:6092070 | C | T | 5 | a0001c0002t0017g0163 a0001c0002t0049g0366 a0001c0002t0057g0338 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.727+1565C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6092070 | |||||||
chr17:6092094 | C | T | 1 | a0001c0001t0008g0259 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.727+1589C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6092094 | |||||||
chr17:6092132 | C | T | 22 | a0001c0001t0004g0341 a0001c0001t0007g0320 a0001c0001t0048g0349 others(19): Show |
22 | HG01070.hp1 HG01109.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.727+1627C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6092132 | |||||||
chr17:6092154 | C | CA | 91 | a0001c0001t0001g0058 a0001c0001t0001g0079 a0001c0001t0001g0080 others(88): Show |
95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.727+1669dupA | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6092154 | ||||||
chr17:6092154 | CA | C | 9 | a0001c0001t0002g0137 a0001c0001t0003g0398 a0001c0002t0004g0167 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.727+1669delA | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6092154 | ||||||
chr17:6092154 | CAA | C | 14 | a0001c0001t0004g0341 a0001c0001t0007g0320 a0001c0001t0048g0349 others(11): Show |
14 | HG01070.hp1 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.727+1668_727+1669d others(4): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6092154 | ||||||
chr17:6092245 | A | G | 1 | a0001c0001t0003g0127 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.727+1740A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6092245 | |||||||
chr17:6092253 | C | T | 7 | a0001c0001t0001g0080 a0001c0001t0001g0272 a0001c0001t0002g0151 others(4): Show |
7 | HG01943.hp1 NA18946.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.727+1748C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6092253 | |||||||
chr17:6092286 | C | T | 4 | a0001c0001t0088g0282 a0002c0006t0015g0111 a0002c0006t0056g0110 others(1): Show |
4 | HG01070.hp1 HG02257.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.727+1781C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6092286 | |||||||
chr17:6092441 | G | T | 2 | a0001c0001t0002g0063 a0001c0001t0002g0064 |
2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.727+1936G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6092441 | |||||||
chr17:6092510 | C | T | 3 | a0001c0002t0017g0163 a0001c0002t0057g0338 a0001c0003t0076g0378 |
3 | HG02572.hp2 HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.727+2005C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6092510 | |||||||
chr17:6092585 | C | T | 1 | a0001c0003t0044g0333 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.727+2080C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6092585 | |||||||
chr17:6092587 | G | A | 5 | a0001c0002t0004g0167 a0001c0002t0014g0375 a0001c0002t0072g0262 others(2): Show |
5 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.727+2082G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6092587 | |||||||
chr17:6093071 | C | T | 13 | a0001c0001t0007g0320 a0001c0001t0088g0282 a0001c0002t0007g0185 others(10): Show |
14 | HG01070.hp1 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.728-2031C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6093071 | |||||||
chr17:6093147 | C | CCTGGGGA others(13): Show |
1 | a0001c0001t0037g0348 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.728-1945_728-1944i others(22): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6093147 | ||||||
chr17:6093167 | G | A | 210 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
220 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.728-1935G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6093167 | |||||||
chr17:6093170 | C | A | 1 | a0001c0004t0004g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.728-1932C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6093170 | |||||||
chr17:6093217 | C | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0058 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.728-1885C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6093217 | |||||||
chr17:6093228 | A | G | 1 | a0001c0020t0003g0138 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.728-1874A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6093228 | |||||||
chr17:6093381 | G | A | 1 | a0001c0002t0001g0092 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.728-1721G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6093381 | |||||||
chr17:6093462 | G | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0058 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.728-1640G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6093462 | |||||||
chr17:6093541 | C | T | 1 | a0002c0006t0005g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.728-1561C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6093541 | |||||||
chr17:6093656 | G | A | 1 | a0001c0002t0075g0181 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.728-1446G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6093656 | |||||||
chr17:6093824 | G | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0058 others(110): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.728-1278G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6093824 | |||||||
chr17:6093962 | T | C | 1 | a0010c0011t0002g0291 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.728-1140T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6093962 | |||||||
chr17:6094133 | C | T | 1 | a0001c0001t0002g0357 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.728-969C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094133 | |||||||
chr17:6094156 | G | A | 48 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0402 others(45): Show |
52 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.728-946G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094156 | |||||||
chr17:6094222 | A | G | 1 | a0001c0002t0013g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.728-880A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094222 | |||||||
chr17:6094301 | T | G | 6 | a0001c0002t0004g0389 a0001c0002t0029g0190 a0001c0003t0014g0256 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.728-801T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094301 | |||||||
chr17:6094376 | G | A | 5 | a0001c0002t0007g0334 a0001c0002t0014g0171 a0001c0002t0062g0173 others(2): Show |
5 | HG02615.hp1 HG02809.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.728-726G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094376 | |||||||
chr17:6094396 | G | A | 1 | a0001c0002t0003g0336 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.728-706G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094396 | |||||||
chr17:6094512 | A | G | 4 | a0001c0002t0029g0190 a0001c0003t0035g0245 a0001c0004t0014g0170 others(1): Show |
4 | HG02280.hp2 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.728-590A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094512 | |||||||
chr17:6094544 | G | A | 1 | a0001c0001t0008g0295 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.728-558G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094544 | |||||||
chr17:6094551 | A | AGAAG | 168 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0058 others(165): Show |
173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.728-535_728-532dup others(4): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6094551 | ||||||
chr17:6094589 | G | C | 1 | a0001c0002t0070g0354 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.728-513G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094589 | |||||||
chr17:6094595 | G | GGAAGGAA others(7): Show |
49 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0402 others(46): Show |
53 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.728-492_728-479dup others(14): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6094595 | ||||||
chr17:6094623 | A | T | 1 | a0001c0004t0004g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.728-479A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094623 | |||||||
chr17:6094627 | T | C | 1 | a0001c0004t0004g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.728-475T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094627 | |||||||
chr17:6094636 | C | T | 2 | a0001c0002t0001g0347 a0001c0002t0004g0342 |
2 | HG00735.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.728-466C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094636 | |||||||
chr17:6094685 | G | T | 103 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0058 others(100): Show |
104 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.728-417G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094685 | |||||||
chr17:6094780 | A | AAGGAAGG others(5): Show |
1 | a0001c0004t0004g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.728-314_728-303dup others(12): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6094780 | ||||||
chr17:6094784 | A | AAGGGAGG others(5): Show |
1 | a0001c0001t0002g0302 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.728-315_728-314ins others(12): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6094784 | ||||||
chr17:6094784 | A | AAGGGAGG others(21): Show |
2 | a0001c0002t0004g0191 a0001c0002t0081g0376 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.728-315_728-314ins others(28): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6094784 | ||||||
chr17:6094796 | A | G | 2 | a0001c0002t0004g0191 a0001c0002t0081g0376 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.728-306A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094796 | |||||||
chr17:6094804 | G | A | 1 | a0001c0001t0011g0134 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.728-298G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094804 | |||||||
chr17:6094808 | A | AAGGGAGG others(93): Show |
1 | a0001c0002t0015g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.728-251_728-250ins others(100): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6094808 | ||||||
chr17:6094808 | A | G | 5 | a0001c0001t0002g0302 a0001c0001t0011g0134 a0001c0002t0004g0191 others(2): Show |
5 | HG02165.hp1 HG02258.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.728-294A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094808 | |||||||
chr17:6094816 | A | G | 3 | a0001c0002t0004g0191 a0001c0002t0081g0376 a0001c0004t0004g0187 |
3 | HG02258.hp2 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.728-286A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094816 | |||||||
chr17:6094838 | G | GGCAGAAG others(93): Show |
2 | a0001c0001t0001g0261 a0001c0002t0018g0214 |
2 | HG01099.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.728-251_728-250ins others(100): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6094838 | ||||||
chr17:6094838 | G | GGCAGAAG others(97): Show |
9 | a0001c0002t0026g0204 a0001c0002t0026g0205 a0003c0005t0014g0193 others(6): Show |
9 | HG02257.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.728-251_728-250ins others(104): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr17 | 6094838 | ||||||
chr17:6094857 | C | T | 1 | a0001c0001t0048g0349 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.728-245C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094857 | |||||||
chr17:6094926 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.728-176T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094926 | |||||||
chr17:6094988 | G | A | 1 | a0001c0004t0004g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.728-114G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094988 | |||||||
chr17:6094992 | CG | C | 12 | a0001c0001t0001g0261 a0001c0002t0015g0054 a0001c0002t0018g0214 others(9): Show |
12 | HG01099.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.728-109delG | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 4/8 | chr17 | 6094992 | |||||||
chr17:6095275 | T | C | 12 | a0001c0001t0001g0261 a0001c0002t0015g0054 a0001c0002t0018g0214 others(9): Show |
12 | HG01099.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+52T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6095275 | |||||||
chr17:6095371 | C | G | 53 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0402 others(50): Show |
57 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.849+148C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6095371 | |||||||
chr17:6095446 | C | T | 1 | a0001c0002t0001g0226 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849+223C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6095446 | |||||||
chr17:6095462 | G | A | 4 | a0001c0003t0031g0206 a0001c0003t0044g0333 a0001c0003t0092g0202 others(1): Show |
4 | HG02647.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+239G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6095462 | |||||||
chr17:6095462 | G | T | 10 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0001t0001g0301 others(7): Show |
10 | HG00621.hp1 HG00673.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.849+239G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6095462 | |||||||
chr17:6095496 | C | G | 3 | a0001c0002t0004g0191 a0001c0002t0081g0376 a0001c0004t0004g0187 |
3 | HG02258.hp2 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.849+273C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6095496 | |||||||
chr17:6095586 | G | A | 12 | a0001c0001t0001g0261 a0001c0002t0015g0054 a0001c0002t0018g0214 others(9): Show |
12 | HG01099.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+363G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6095586 | |||||||
chr17:6095595 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0058 others(112): Show |
116 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.849+372G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6095595 | |||||||
chr17:6095623 | G | A | 1 | a0001c0002t0007g0334 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.849+400G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6095623 | |||||||
chr17:6095648 | G | A | 2 | a0001c0004t0014g0170 a0003c0005t0079g0385 |
2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.849+425G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6095648 | |||||||
chr17:6095673 | C | T | 6 | a0001c0002t0007g0185 a0001c0002t0013g0009 a0001c0002t0013g0049 others(3): Show |
7 | HG02818.hp2 HG02965.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.849+450C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6095673 | |||||||
chr17:6095721 | G | A | 1 | a0001c0004t0004g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+498G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6095721 | |||||||
chr17:6096218 | C | T | 1 | a0001c0001t0035g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.849+995C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096218 | |||||||
chr17:6096260 | G | T | 3 | a0001c0001t0003g0216 a0001c0001t0004g0346 a0001c0004t0041g0120 |
3 | HG01255.hp2 HG01257.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.849+1037G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096260 | |||||||
chr17:6096321 | T | C | 2 | a0001c0003t0004g0194 a0001c0003t0004g0195 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.849+1098T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096321 | |||||||
chr17:6096354 | C | T | 1 | a0002c0006t0015g0111 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.849+1131C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096354 | |||||||
chr17:6096466 | C | T | 1 | a0001c0001t0003g0074 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.849+1243C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096466 | |||||||
chr17:6096473 | T | C | 13 | a0001c0001t0007g0320 a0001c0001t0088g0282 a0001c0002t0007g0185 others(10): Show |
14 | HG01070.hp1 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.849+1250T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096473 | |||||||
chr17:6096480 | G | A | 1 | a0001c0002t0004g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.849+1257G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096480 | |||||||
chr17:6096551 | C | T | 6 | a0001c0001t0001g0040 a0001c0002t0001g0388 a0001c0002t0003g0099 others(3): Show |
6 | HG00639.hp2 HG00738.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+1328C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096551 | |||||||
chr17:6096581 | T | A | 266 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.849+1358T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096581 | |||||||
chr17:6096785 | C | G | 56 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0094 others(53): Show |
61 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.849+1562C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096785 | |||||||
chr17:6096790 | C | G | 52 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0094 others(49): Show |
57 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.849+1567C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096790 | |||||||
chr17:6096879 | T | G | 1 | a0001c0001t0002g0302 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.849+1656T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096879 | |||||||
chr17:6096905 | T | G | 2 | a0001c0003t0004g0194 a0001c0003t0004g0195 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.849+1682T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096905 | |||||||
chr17:6096969 | G | A | 10 | a0001c0001t0001g0261 a0001c0002t0015g0054 a0001c0002t0026g0204 others(7): Show |
10 | HG01099.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.849+1746G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6096969 | |||||||
chr17:6097042 | A | T | 1 | a0003c0005t0079g0385 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.849+1819A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097042 | |||||||
chr17:6097043 | A | T | 1 | a0003c0005t0079g0385 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.849+1820A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097043 | |||||||
chr17:6097048 | A | T | 1 | a0003c0005t0079g0385 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.849+1825A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097048 | |||||||
chr17:6097108 | G | T | 1 | a0001c0001t0058g0133 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.849+1885G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097108 | |||||||
chr17:6097208 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0040 others(97): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.849+1985G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097208 | |||||||
chr17:6097248 | C | G | 1 | a0001c0002t0075g0181 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.849+2025C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097248 | |||||||
chr17:6097272 | G | A | 32 | a0001c0001t0001g0040 a0001c0001t0002g0063 a0001c0001t0002g0064 others(29): Show |
32 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.849+2049G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097272 | |||||||
chr17:6097328 | A | G | 218 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(215): Show |
228 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.849+2105A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097328 | |||||||
chr17:6097419 | T | A | 67 | a0001c0001t0001g0094 a0001c0001t0001g0107 a0001c0001t0001g0128 others(64): Show |
72 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.849+2196T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097419 | |||||||
chr17:6097431 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0046 others(37): Show |
43 | HG00408.hp2 HG00609.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.849+2208T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097431 | |||||||
chr17:6097518 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.849+2295G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097518 | |||||||
chr17:6097529 | T | C | 16 | a0001c0001t0002g0302 a0001c0001t0007g0320 a0001c0001t0088g0282 others(13): Show |
17 | HG01070.hp1 HG02165.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.849+2306T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097529 | |||||||
chr17:6097536 | C | T | 18 | a0001c0002t0004g0167 a0001c0002t0004g0191 a0001c0002t0014g0375 others(15): Show |
18 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.849+2313C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097536 | |||||||
chr17:6097539 | C | T | 1 | a0001c0003t0004g0194 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.849+2316C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097539 | |||||||
chr17:6097541 | C | T | 1 | a0001c0001t0002g0302 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.849+2318C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097541 | |||||||
chr17:6097542 | G | A | 5 | a0001c0002t0015g0174 a0001c0002t0023g0188 a0001c0002t0025g0383 others(2): Show |
5 | HG01167.hp1 HG01243.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+2319G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097542 | |||||||
chr17:6097644 | C | T | 1 | a0001c0001t0024g0197 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.849+2421C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097644 | |||||||
chr17:6097645 | G | A | 2 | a0004c0010t0040g0042 a0004c0010t0040g0043 |
2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.849+2422G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097645 | |||||||
chr17:6097685 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0272 a0001c0001t0002g0269 others(2): Show |
5 | NA18963.hp2 NA18981.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+2462G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097685 | |||||||
chr17:6097705 | T | C | 1 | a0001c0001t0001g0356 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.849+2482T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097705 | |||||||
chr17:6097904 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.849+2681C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097904 | |||||||
chr17:6097952 | C | CT | 7 | a0001c0001t0001g0145 a0001c0001t0003g0147 a0001c0001t0003g0397 others(4): Show |
7 | HG01175.hp1 HG01175.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.849+2745dupT | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr17 | 6097952 | ||||||
chr17:6097954 | T | TC | 144 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0040 others(141): Show |
146 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.849+2731_849+2732i others(3): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097954 | |||||||
chr17:6097955 | T | C | 4 | a0001c0001t0001g0058 a0001c0001t0010g0323 a0001c0004t0032g0371 others(1): Show |
4 | HG01070.hp1 NA18957.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+2732T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6097955 | |||||||
chr17:6098041 | C | T | 1 | a0001c0001t0002g0364 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.849+2818C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6098041 | |||||||
chr17:6098118 | T | C | 4 | a0001c0001t0028g0265 a0001c0001t0038g0060 a0001c0001t0047g0086 others(1): Show |
4 | NA18988.hp2 NA19054.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+2895T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6098118 | |||||||
chr17:6098156 | T | TCG | 39 | a0001c0001t0001g0094 a0001c0001t0001g0107 a0001c0001t0001g0128 others(36): Show |
41 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.849+2933_849+2934i others(4): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6098156 | |||||||
chr17:6098156 | T | TG | 133 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(130): Show |
136 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.849+2941dupG | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr17 | 6098156 | ||||||
chr17:6098156 | T | TGG | 37 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0324 others(34): Show |
37 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.849+2940_849+2941d others(4): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr17 | 6098156 | ||||||
chr17:6098373 | C | T | 2 | a0001c0002t0004g0191 a0001c0002t0081g0376 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.849+3150C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6098373 | |||||||
chr17:6098394 | T | G | 2 | a0001c0002t0004g0191 a0001c0002t0081g0376 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.849+3171T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6098394 | |||||||
chr17:6098598 | C | G | 221 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
231 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.849+3375C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6098598 | |||||||
chr17:6098635 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.849+3412G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6098635 | |||||||
chr17:6098648 | G | A | 4 | a0001c0002t0017g0163 a0001c0002t0057g0338 a0001c0003t0076g0378 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+3425G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6098648 | |||||||
chr17:6098806 | T | C | 1 | a0001c0003t0089g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.849+3583T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6098806 | |||||||
chr17:6098908 | A | C | 9 | a0001c0001t0001g0053 a0001c0001t0001g0108 a0001c0001t0001g0324 others(6): Show |
9 | HG00544.hp2 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.849+3685A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6098908 | |||||||
chr17:6098939 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0053 others(90): Show |
95 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.849+3716A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6098939 | |||||||
chr17:6098981 | T | C | 1 | a0001c0001t0002g0302 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.849+3758T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6098981 | |||||||
chr17:6099000 | A | G | 1 | a0001c0002t0004g0342 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.849+3777A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6099000 | |||||||
chr17:6099067 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0052 others(16): Show |
21 | HG00323.hp1 HG00639.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.849+3844C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6099067 | |||||||
chr17:6099068 | TTGG | T | 48 | a0001c0001t0001g0040 a0001c0001t0001g0094 a0001c0001t0001g0158 others(45): Show |
49 | HG00544.hp1 HG01069.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.849+3846_849+3848d others(5): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6099068 | |||||||
chr17:6099069 | TGGG | T | 183 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
193 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.849+3850_849+3852d others(5): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr17 | 6099069 | ||||||
chr17:6099072 | G | C | 48 | a0001c0001t0001g0040 a0001c0001t0001g0094 a0001c0001t0001g0158 others(45): Show |
49 | HG00544.hp1 HG01069.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.849+3849G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6099072 | |||||||
chr17:6099112 | T | G | 1 | a0001c0004t0007g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.849+3889T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6099112 | |||||||
chr17:6099165 | G | A | 1 | a0002c0007t0023g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.849+3942G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6099165 | |||||||
chr17:6099428 | T | C | 178 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(175): Show |
188 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.849+4205T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6099428 | |||||||
chr17:6099477 | C | T | 25 | a0001c0001t0001g0261 a0001c0002t0004g0167 a0001c0002t0004g0389 others(22): Show |
25 | HG01099.hp1 HG01167.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.849+4254C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6099477 | |||||||
chr17:6099520 | CA | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0053 others(95): Show |
99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.849+4308delA | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr17 | 6099520 | ||||||
chr17:6099621 | C | T | 2 | a0001c0002t0087g0293 a0001c0016t0003g0230 |
2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.849+4398C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6099621 | |||||||
chr17:6099713 | A | C | 1 | a0001c0001t0005g0305 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.849+4490A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6099713 | |||||||
chr17:6099761 | T | C | 409 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(406): Show |
425 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(422): Show |
intron_variant | MODIFIER | c.849+4538T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6099761 | |||||||
chr17:6099843 | C | A | 236 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.849+4620C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6099843 | |||||||
chr17:6100020 | T | C | 1 | a0001c0001t0002g0302 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.849+4797T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100020 | |||||||
chr17:6100136 | A | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0053 others(95): Show |
99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.849+4913A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100136 | |||||||
chr17:6100142 | G | T | 10 | a0001c0001t0088g0282 a0001c0002t0007g0185 a0001c0002t0013g0009 others(7): Show |
11 | HG01070.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.849+4919G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100142 | |||||||
chr17:6100444 | G | A | 2 | a0004c0010t0040g0042 a0004c0010t0040g0043 |
2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.849+5221G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100444 | |||||||
chr17:6100461 | C | T | 6 | a0001c0002t0007g0242 a0001c0002t0015g0054 a0001c0002t0023g0188 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+5238C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100461 | |||||||
chr17:6100469 | G | A | 8 | a0001c0001t0001g0073 a0001c0001t0002g0362 a0001c0001t0021g0075 others(5): Show |
8 | HG00423.hp2 HG00558.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.849+5246G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100469 | |||||||
chr17:6100526 | G | A | 1 | a0001c0002t0007g0244 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.849+5303G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100526 | |||||||
chr17:6100568 | T | C | 357 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(354): Show |
370 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.849+5345T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100568 | |||||||
chr17:6100612 | G | A | 1 | a0003c0005t0014g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.849+5389G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100612 | |||||||
chr17:6100772 | G | A | 5 | a0001c0002t0017g0015 a0001c0002t0020g0192 a0001c0002t0023g0243 others(2): Show |
5 | HG02559.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+5549G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100772 | |||||||
chr17:6100897 | A | G | 279 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(276): Show |
290 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.849+5674A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100897 | |||||||
chr17:6100948 | T | C | 357 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(354): Show |
370 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.849+5725T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100948 | |||||||
chr17:6100961 | T | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0053 others(68): Show |
72 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.849+5738T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6100961 | |||||||
chr17:6101044 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.849+5821C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101044 | |||||||
chr17:6101060 | G | C | 1 | a0001c0001t0045g0123 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.849+5837G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101060 | |||||||
chr17:6101137 | A | C | 1 | a0003c0005t0074g0387 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.849+5914A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101137 | |||||||
chr17:6101319 | T | C | 231 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
242 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.849+6096T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101319 | |||||||
chr17:6101326 | A | AG | 4 | a0001c0001t0002g0302 a0003c0005t0074g0387 a0004c0010t0040g0042 others(1): Show |
4 | HG02165.hp1 HG02257.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+6104dupG | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr17 | 6101326 | ||||||
chr17:6101385 | C | T | 1 | a0001c0003t0007g0326 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.849+6162C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101385 | |||||||
chr17:6101538 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0058 others(78): Show |
82 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.849+6315C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101538 | |||||||
chr17:6101539 | G | A | 2 | a0004c0010t0040g0042 a0004c0010t0040g0043 |
2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.849+6316G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101539 | |||||||
chr17:6101583 | A | G | 11 | a0001c0002t0004g0389 a0001c0002t0007g0242 a0001c0002t0013g0165 others(8): Show |
11 | HG01167.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.849+6360A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101583 | |||||||
chr17:6101676 | G | C | 1 | a0001c0002t0072g0262 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.849+6453G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101676 | |||||||
chr17:6101704 | C | T | 2 | a0001c0001t0008g0286 a0001c0002t0003g0336 |
2 | HG01496.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.849+6481C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101704 | |||||||
chr17:6101731 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0053 others(84): Show |
88 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.849+6508A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101731 | |||||||
chr17:6101795 | G | A | 1 | a0001c0004t0004g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849+6572G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101795 | |||||||
chr17:6101926 | C | G | 52 | a0001c0001t0001g0040 a0001c0001t0001g0094 a0001c0001t0001g0158 others(49): Show |
53 | HG00544.hp1 HG01069.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.849+6703C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101926 | |||||||
chr17:6101965 | C | G | 2 | a0001c0001t0001g0400 a0001c0001t0002g0095 |
2 | NA18979.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.849+6742C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6101965 | |||||||
chr17:6102036 | G | A | 55 | a0001c0001t0001g0040 a0001c0001t0001g0094 a0001c0001t0001g0158 others(52): Show |
56 | HG00544.hp1 HG01069.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.849+6813G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6102036 | |||||||
chr17:6102049 | G | A | 2 | a0001c0003t0004g0194 a0001c0003t0004g0195 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.849+6826G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6102049 | |||||||
chr17:6102209 | A | G | 1 | a0001c0001t0002g0302 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.849+6986A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6102209 | |||||||
chr17:6102295 | C | T | 1 | a0001c0001t0005g0369 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+7072C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6102295 | |||||||
chr17:6102329 | G | C | 2 | a0001c0002t0022g0047 a0003c0005t0079g0385 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.849+7106G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6102329 | |||||||
chr17:6102364 | C | T | 1 | a0001c0002t0004g0342 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.849+7141C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6102364 | |||||||
chr17:6102501 | C | A | 1 | a0001c0002t0001g0227 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.850-7106C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6102501 | |||||||
chr17:6102507 | A | G | 1 | a0001c0002t0004g0374 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.850-7100A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6102507 | |||||||
chr17:6102666 | C | T | 1 | a0001c0001t0006g0131 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.850-6941C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6102666 | |||||||
chr17:6102730 | A | C | 1 | a0001c0002t0017g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.850-6877A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6102730 | |||||||
chr17:6102770 | C | T | 2 | a0001c0002t0010g0176 a0001c0002t0067g0175 |
2 | NA18962.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.850-6837C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6102770 | |||||||
chr17:6102816 | C | T | 1 | a0001c0023t0001g0026 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.850-6791C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6102816 | |||||||
chr17:6103130 | C | T | 1 | a0001c0002t0015g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.850-6477C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6103130 | |||||||
chr17:6103137 | T | C | 387 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(384): Show |
401 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(398): Show |
intron_variant | MODIFIER | c.850-6470T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6103137 | |||||||
chr17:6103444 | A | T | 1 | a0001c0001t0071g0098 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.850-6163A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6103444 | |||||||
chr17:6103445 | C | A | 1 | a0001c0001t0071g0098 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.850-6162C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6103445 | |||||||
chr17:6103555 | C | T | 2 | a0001c0003t0001g0236 a0001c0018t0018g0335 |
2 | HG01106.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.850-6052C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6103555 | |||||||
chr17:6103613 | C | A | 2 | a0004c0010t0040g0042 a0004c0010t0040g0043 |
2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.850-5994C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6103613 | |||||||
chr17:6103694 | C | T | 1 | a0002c0007t0003g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.850-5913C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6103694 | |||||||
chr17:6103725 | T | A | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | NA18946.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.850-5882T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6103725 | |||||||
chr17:6103824 | G | A | 303 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(300): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.850-5783G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6103824 | |||||||
chr17:6103880 | A | T | 5 | a0001c0003t0004g0194 a0001c0003t0004g0195 a0003c0005t0074g0387 others(2): Show |
5 | HG02257.hp2 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-5727A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6103880 | |||||||
chr17:6104035 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.850-5572A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6104035 | |||||||
chr17:6104051 | C | G | 1 | a0001c0002t0001g0226 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.850-5556C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6104051 | |||||||
chr17:6104075 | G | A | 3 | a0001c0001t0002g0199 a0001c0001t0012g0198 a0001c0001t0012g0215 |
3 | HG01069.hp2 HG01106.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.850-5532G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6104075 | |||||||
chr17:6104185 | C | T | 2 | a0001c0002t0025g0383 a0001c0002t0078g0384 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.850-5422C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6104185 | |||||||
chr17:6104518 | A | T | 1 | a0001c0001t0002g0302 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.850-5089A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6104518 | |||||||
chr17:6104519 | C | G | 1 | a0001c0002t0026g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.850-5088C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6104519 | |||||||
chr17:6104632 | G | C | 1 | a0001c0004t0032g0371 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.850-4975G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6104632 | |||||||
chr17:6104715 | A | T | 1 | a0001c0001t0001g0128 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.850-4892A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6104715 | |||||||
chr17:6104747 | A | T | 1 | a0010c0011t0002g0291 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.850-4860A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6104747 | |||||||
chr17:6104796 | G | A | 1 | a0001c0002t0001g0222 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.850-4811G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6104796 | |||||||
chr17:6104824 | G | A | 2 | a0001c0002t0007g0244 a0002c0007t0090g0184 |
2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.850-4783G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6104824 | |||||||
chr17:6105032 | C | T | 2 | a0001c0001t0002g0124 a0001c0001t0005g0017 |
3 | HG01257.hp1 HG01258.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.850-4575C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6105032 | |||||||
chr17:6105218 | G | A | 1 | a0001c0004t0082g0258 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.850-4389G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6105218 | |||||||
chr17:6105276 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.850-4331C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6105276 | |||||||
chr17:6105411 | A | G | 252 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(249): Show |
263 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(260): Show |
intron_variant | MODIFIER | c.850-4196A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6105411 | |||||||
chr17:6105452 | A | G | 1 | a0001c0001t0002g0302 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.850-4155A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6105452 | |||||||
chr17:6105539 | T | C | 1 | a0001c0004t0082g0258 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.850-4068T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6105539 | |||||||
chr17:6105570 | G | T | 1 | a0001c0001t0001g0329 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.850-4037G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6105570 | |||||||
chr17:6105585 | T | C | 1 | a0001c0001t0001g0356 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.850-4022T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6105585 | |||||||
chr17:6105683 | G | A | 2 | a0001c0003t0001g0236 a0001c0018t0018g0335 |
2 | HG01106.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.850-3924G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6105683 | |||||||
chr17:6105843 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(263): Show |
277 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.850-3764A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6105843 | |||||||
chr17:6105901 | G | A | 1 | a0002c0007t0003g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.850-3706G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6105901 | |||||||
chr17:6105986 | T | C | 250 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(247): Show |
261 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.850-3621T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6105986 | |||||||
chr17:6106112 | A | G | 2 | a0001c0002t0001g0350 a0001c0002t0001g0351 |
2 | HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.850-3495A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106112 | |||||||
chr17:6106146 | C | T | 1 | a0003c0005t0014g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.850-3461C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106146 | |||||||
chr17:6106154 | T | C | 2 | a0001c0001t0001g0285 a0001c0001t0002g0095 |
2 | HG02071.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.850-3453T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106154 | |||||||
chr17:6106292 | A | T | 39 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0094 others(36): Show |
41 | HG00544.hp1 HG01069.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.850-3315A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106292 | |||||||
chr17:6106402 | A | G | 1 | a0001c0001t0048g0349 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850-3205A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106402 | |||||||
chr17:6106455 | C | T | 2 | a0001c0003t0004g0194 a0001c0003t0004g0195 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.850-3152C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106455 | |||||||
chr17:6106466 | T | G | 6 | a0001c0002t0004g0389 a0001c0002t0015g0174 a0001c0002t0029g0190 others(3): Show |
6 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-3141T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106466 | |||||||
chr17:6106480 | T | A | 2 | a0001c0002t0007g0244 a0002c0007t0090g0184 |
2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.850-3127T>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106480 | |||||||
chr17:6106529 | A | G | 1 | a0001c0001t0003g0007 | 2 | HG00099.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.850-3078A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106529 | |||||||
chr17:6106549 | T | C | 1 | a0001c0004t0007g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.850-3058T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106549 | |||||||
chr17:6106563 | C | A | 1 | a0001c0002t0005g0212 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.850-3044C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106563 | |||||||
chr17:6106636 | C | T | 187 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 others(184): Show |
196 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.850-2971C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106636 | |||||||
chr17:6106709 | G | T | 4 | a0001c0002t0004g0374 a0001c0002t0007g0244 a0002c0007t0003g0168 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-2898G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106709 | |||||||
chr17:6106774 | A | T | 1 | a0003c0005t0014g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.850-2833A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106774 | |||||||
chr17:6106802 | C | T | 1 | a0001c0001t0045g0123 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.850-2805C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106802 | |||||||
chr17:6106886 | C | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(296): Show |
312 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.850-2721C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106886 | |||||||
chr17:6106932 | A | T | 16 | a0001c0001t0004g0341 a0001c0001t0035g0035 a0001c0001t0048g0349 others(13): Show |
16 | HG01109.hp2 HG02451.hp2 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.850-2675A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6106932 | |||||||
chr17:6107281 | A | T | 3 | a0002c0006t0007g0166 a0002c0006t0015g0111 a0002c0007t0023g0038 |
3 | HG01109.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.850-2326A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107281 | |||||||
chr17:6107310 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.850-2297G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107310 | |||||||
chr17:6107315 | A | G | 1 | a0001c0004t0007g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.850-2292A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107315 | |||||||
chr17:6107367 | G | A | 1 | a0001c0002t0023g0243 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.850-2240G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107367 | |||||||
chr17:6107455 | C | T | 4 | a0001c0001t0004g0341 a0001c0001t0035g0035 a0001c0001t0048g0349 others(1): Show |
4 | HG02723.hp2 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-2152C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107455 | |||||||
chr17:6107512 | GA | G | 5 | a0001c0001t0004g0341 a0001c0001t0035g0035 a0001c0001t0048g0349 others(2): Show |
5 | HG01891.hp1 HG02723.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-2085delA | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr17 | 6107512 | ||||||
chr17:6107558 | C | T | 1 | a0001c0004t0007g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.850-2049C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107558 | |||||||
chr17:6107769 | G | A | 2 | a0001c0002t0025g0383 a0001c0003t0001g0236 |
2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.850-1838G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107769 | |||||||
chr17:6107791 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.850-1816G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107791 | |||||||
chr17:6107882 | A | G | 1 | a0001c0004t0007g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.850-1725A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107882 | |||||||
chr17:6107890 | G | T | 4 | a0001c0001t0004g0341 a0001c0001t0035g0035 a0001c0001t0048g0349 others(1): Show |
4 | HG02723.hp2 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-1717G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107890 | |||||||
chr17:6107920 | T | C | 1 | a0001c0002t0004g0316 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.850-1687T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107920 | |||||||
chr17:6107933 | C | G | 45 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0052 others(42): Show |
46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.850-1674C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107933 | |||||||
chr17:6107968 | C | T | 1 | a0001c0004t0007g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.850-1639C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107968 | |||||||
chr17:6107981 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0003g0397 a0001c0002t0009g0229 |
3 | HG01081.hp2 HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.850-1626T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107981 | |||||||
chr17:6107996 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(266): Show |
281 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.850-1611A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6107996 | |||||||
chr17:6108069 | G | C | 2 | a0001c0003t0044g0333 a0001c0016t0003g0230 |
2 | HG03453.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.850-1538G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6108069 | |||||||
chr17:6108078 | G | A | 1 | a0001c0003t0089g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.850-1529G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6108078 | |||||||
chr17:6108188 | C | T | 1 | a0002c0006t0056g0110 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.850-1419C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6108188 | |||||||
chr17:6108378 | C | T | 2 | a0001c0001t0004g0346 a0001c0002t0008g0247 |
2 | HG01358.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.850-1229C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6108378 | |||||||
chr17:6108446 | A | G | 407 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(404): Show |
423 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(420): Show |
intron_variant | MODIFIER | c.850-1161A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6108446 | |||||||
chr17:6108797 | A | G | 5 | a0001c0003t0007g0326 a0001c0003t0076g0378 a0001c0003t0092g0202 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-810A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6108797 | |||||||
chr17:6108885 | G | C | 2 | a0001c0001t0001g0014 a0001c0001t0006g0014 |
2 | NA19009.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.850-722G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6108885 | |||||||
chr17:6108941 | G | C | 1 | a0001c0001t0001g0275 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.850-666G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6108941 | |||||||
chr17:6108964 | A | G | 1 | a0001c0002t0001g0213 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.850-643A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6108964 | |||||||
chr17:6108988 | G | T | 2 | a0001c0003t0089g0203 a0001c0004t0014g0170 |
2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.850-619G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6108988 | |||||||
chr17:6109069 | A | G | 11 | a0001c0001t0007g0320 a0001c0002t0015g0036 a0001c0002t0023g0188 others(8): Show |
11 | HG01891.hp1 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.850-538A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6109069 | |||||||
chr17:6109081 | C | T | 5 | a0001c0001t0007g0320 a0001c0002t0015g0036 a0001c0002t0023g0188 others(2): Show |
5 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-526C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6109081 | |||||||
chr17:6109133 | C | T | 1 | a0001c0002t0002g0142 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.850-474C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6109133 | |||||||
chr17:6109156 | A | T | 11 | a0001c0001t0007g0320 a0001c0002t0015g0036 a0001c0002t0023g0188 others(8): Show |
11 | HG01891.hp1 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.850-451A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6109156 | |||||||
chr17:6109173 | C | T | 1 | a0001c0001t0003g0249 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.850-434C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6109173 | |||||||
chr17:6109177 | C | G | 2 | a0001c0003t0044g0333 a0001c0016t0003g0230 |
2 | HG03453.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.850-430C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6109177 | |||||||
chr17:6109181 | G | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0108 a0001c0001t0005g0101 others(10): Show |
13 | HG00438.hp1 HG01243.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.850-426G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6109181 | |||||||
chr17:6109200 | A | G | 1 | a0001c0002t0001g0208 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.850-407A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6109200 | |||||||
chr17:6109202 | A | G | 7 | a0001c0002t0007g0185 a0001c0002t0007g0334 a0001c0002t0013g0009 others(4): Show |
8 | HG02818.hp2 HG02965.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-405A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6109202 | |||||||
chr17:6109225 | C | A | 1 | a0001c0004t0003g0308 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.850-382C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6109225 | |||||||
chr17:6109521 | G | A | 1 | a0001c0001t0030g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.850-86G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6109521 | |||||||
chr17:6109595 | G | A | 2 | a0001c0001t0001g0022 a0001c0002t0003g0177 |
3 | HG03490.hp2 HG03492.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.850-12G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 5/8 | chr17 | 6109595 | |||||||
chr17:6110213 | C | A | 18 | a0001c0001t0004g0341 a0001c0001t0007g0320 a0001c0001t0035g0035 others(15): Show |
18 | HG01891.hp1 HG02258.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1009+447C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 6/8 | chr17 | 6110213 | |||||||
chr17:6110214 | G | A | 3 | a0001c0002t0020g0192 a0003c0005t0020g0343 a0003c0005t0020g0345 |
3 | HG02486.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1009+448G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 6/8 | chr17 | 6110214 | |||||||
chr17:6110220 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1009+454G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 6/8 | chr17 | 6110220 | |||||||
chr17:6110307 | C | T | 1 | a0001c0003t0044g0333 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1010-464C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 6/8 | chr17 | 6110307 | |||||||
chr17:6110514 | G | A | 2 | a0001c0003t0044g0333 a0001c0016t0003g0230 |
2 | HG03453.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1010-257G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 6/8 | chr17 | 6110514 | |||||||
chr17:6110540 | A | G | 4 | a0001c0002t0004g0389 a0001c0003t0014g0256 a0001c0003t0031g0206 others(1): Show |
4 | HG02055.hp1 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1010-231A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 6/8 | chr17 | 6110540 | |||||||
chr17:6110682 | C | T | 4 | a0001c0001t0004g0341 a0001c0001t0035g0035 a0001c0001t0048g0349 others(1): Show |
4 | HG02723.hp2 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1010-89C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 6/8 | chr17 | 6110682 | |||||||
chr17:6110739 | G | C | 1 | a0001c0003t0001g0218 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1010-32G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 6/8 | chr17 | 6110739 | |||||||
chr17:6111080 | GCCATACT others(3): Show |
G | 343 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(340): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.1174+148_1174+157d others(12): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | 6111080 | ||||||
chr17:6111102 | T | C | 26 | a0001c0001t0001g0161 a0001c0001t0008g0259 a0001c0001t0050g0250 others(23): Show |
26 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1174+167T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111102 | |||||||
chr17:6111123 | G | T | 3 | a0001c0001t0002g0269 a0001c0001t0002g0362 a0001c0002t0016g0332 |
3 | HG00423.hp2 HG02155.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1174+188G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111123 | |||||||
chr17:6111340 | A | G | 1 | a0001c0003t0014g0256 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1174+405A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111340 | |||||||
chr17:6111427 | G | A | 1 | a0001c0002t0001g0032 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1174+492G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111427 | |||||||
chr17:6111439 | G | C | 3 | a0001c0003t0014g0256 a0001c0003t0031g0206 a0001c0003t0035g0245 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1174+504G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111439 | |||||||
chr17:6111453 | C | T | 18 | a0001c0003t0001g0045 a0001c0003t0001g0218 a0001c0003t0001g0236 others(15): Show |
18 | HG00544.hp1 HG00621.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1174+518C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111453 | |||||||
chr17:6111514 | A | C | 1 | a0001c0002t0055g0152 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1174+579A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111514 | |||||||
chr17:6111535 | T | G | 1 | a0001c0001t0005g0369 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1174+600T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111535 | |||||||
chr17:6111700 | CA | C | 11 | a0001c0001t0001g0052 a0001c0001t0001g0162 a0001c0001t0001g0372 others(8): Show |
11 | HG01516.hp1 HG01516.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174+789delA | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | 6111700 | ||||||
chr17:6111700 | CAAAAAAA others(8): Show |
C | 2 | a0001c0002t0087g0293 a0001c0016t0003g0230 |
2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1174+775_1174+789d others(17): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | 6111700 | ||||||
chr17:6111724 | A | AG | 14 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0238 others(11): Show |
15 | HG00423.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1174+790dupG | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | 6111724 | ||||||
chr17:6111724 | A | G | 312 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(309): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1174+789A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111724 | |||||||
chr17:6111757 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0402 a0001c0001t0006g0157 others(1): Show |
4 | NA18972.hp1 NA19009.hp2 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+822C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111757 | |||||||
chr17:6111773 | A | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
8 | HG01175.hp2 HG01975.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174+838A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111773 | |||||||
chr17:6111824 | A | C | 1 | a0001c0001t0002g0302 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1174+889A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111824 | |||||||
chr17:6111873 | A | G | 2 | a0001c0004t0004g0187 a0005c0021t0004g0154 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1174+938A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6111873 | |||||||
chr17:6112420 | A | C | 25 | a0001c0001t0001g0161 a0001c0001t0008g0259 a0001c0001t0050g0250 others(22): Show |
25 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1174+1485A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6112420 | |||||||
chr17:6112447 | C | G | 1 | a0001c0001t0035g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1174+1512C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6112447 | |||||||
chr17:6112513 | T | C | 1 | a0001c0001t0024g0178 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1174+1578T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6112513 | |||||||
chr17:6112604 | A | C | 1 | a0001c0002t0004g0389 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1174+1669A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6112604 | |||||||
chr17:6112690 | C | CG | 3 | a0001c0001t0002g0309 a0001c0002t0016g0332 a0001c0002t0078g0384 |
3 | HG00423.hp2 HG01243.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1174+1757dupG | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | 6112690 | ||||||
chr17:6112734 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1174+1799T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6112734 | |||||||
chr17:6112745 | A | T | 1 | a0001c0001t0003g0030 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1174+1810A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6112745 | |||||||
chr17:6113078 | G | A | 1 | a0001c0016t0003g0230 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1174+2143G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113078 | |||||||
chr17:6113093 | A | C | 1 | a0003c0005t0022g0344 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1174+2158A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113093 | |||||||
chr17:6113220 | G | A | 1 | a0001c0004t0007g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1174+2285G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113220 | |||||||
chr17:6113290 | A | G | 5 | a0001c0003t0007g0326 a0001c0003t0076g0378 a0001c0003t0092g0202 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174+2355A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113290 | |||||||
chr17:6113299 | A | G | 1 | a0001c0002t0001g0057 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1174+2364A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113299 | |||||||
chr17:6113316 | C | T | 8 | a0001c0002t0004g0316 a0001c0002t0007g0185 a0001c0002t0007g0334 others(5): Show |
9 | HG02818.hp2 HG02886.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174+2381C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113316 | |||||||
chr17:6113401 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0361 others(3): Show |
6 | HG00609.hp2 HG00673.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174+2466C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113401 | |||||||
chr17:6113402 | G | A | 1 | a0001c0002t0002g0104 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1174+2467G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113402 | |||||||
chr17:6113499 | T | G | 389 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(386): Show |
405 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(402): Show |
intron_variant | MODIFIER | c.1174+2564T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113499 | |||||||
chr17:6113640 | A | G | 1 | a0001c0002t0057g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1174+2705A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113640 | |||||||
chr17:6113687 | A | G | 10 | a0001c0001t0007g0320 a0001c0002t0015g0036 a0001c0002t0023g0188 others(7): Show |
10 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1174+2752A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113687 | |||||||
chr17:6113700 | A | C | 17 | a0001c0001t0001g0046 a0001c0001t0001g0069 a0001c0001t0001g0080 others(14): Show |
17 | HG00609.hp1 HG01952.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.1174+2765A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113700 | |||||||
chr17:6113785 | A | C | 362 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(359): Show |
378 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.1174+2850A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113785 | |||||||
chr17:6113800 | G | A | 10 | a0001c0001t0007g0320 a0001c0002t0015g0036 a0001c0002t0023g0188 others(7): Show |
10 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1174+2865G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113800 | |||||||
chr17:6113971 | C | G | 2 | a0001c0002t0087g0293 a0001c0016t0003g0230 |
2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1174+3036C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6113971 | |||||||
chr17:6114124 | G | A | 2 | a0001c0001t0003g0013 a0001c0009t0003g0013 |
2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1174+3189G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6114124 | |||||||
chr17:6114153 | T | TA | 344 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(341): Show |
360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.1174+3237dupA | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | 6114153 | ||||||
chr17:6114153 | T | TAA | 23 | a0001c0001t0001g0069 a0001c0001t0003g0013 a0001c0001t0005g0305 others(20): Show |
23 | HG00323.hp1 HG01256.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1174+3236_1174+323 others(6): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | 6114153 | ||||||
chr17:6114225 | T | C | 2 | a0001c0001t0001g0373 a0001c0001t0002g0066 |
2 | NA18946.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1174+3290T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6114225 | |||||||
chr17:6114400 | G | A | 2 | a0001c0002t0087g0293 a0001c0016t0003g0230 |
2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1174+3465G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6114400 | |||||||
chr17:6114407 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1174+3472A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6114407 | |||||||
chr17:6114420 | C | T | 361 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(358): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.1174+3485C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6114420 | |||||||
chr17:6114460 | ATAAT | A | 3 | a0001c0001t0003g0013 a0001c0002t0005g0231 a0001c0009t0003g0013 |
3 | HG00323.hp1 HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1175-3526_1175-352 others(8): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | 6114460 | ||||||
chr17:6114540 | G | A | 49 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0001g0096 others(46): Show |
49 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1175-3448G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6114540 | |||||||
chr17:6114613 | C | T | 293 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(290): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1175-3375C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6114613 | |||||||
chr17:6114636 | C | T | 1 | a0001c0001t0002g0355 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1175-3352C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6114636 | |||||||
chr17:6114640 | C | T | 1 | a0001c0020t0003g0138 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1175-3348C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6114640 | |||||||
chr17:6114641 | A | G | 403 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(400): Show |
419 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(416): Show |
intron_variant | MODIFIER | c.1175-3347A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6114641 | |||||||
chr17:6114725 | C | T | 2 | a0001c0002t0002g0104 a0001c0002t0032g0106 |
2 | NA18992.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1175-3263C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6114725 | |||||||
chr17:6114745 | G | A | 361 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(358): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.1175-3243G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6114745 | |||||||
chr17:6115061 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0087 others(51): Show |
56 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1175-2927A>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6115061 | |||||||
chr17:6115173 | G | A | 216 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 others(213): Show |
227 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1175-2815G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6115173 | |||||||
chr17:6115330 | C | T | 3 | a0001c0004t0003g0308 a0001c0004t0011g0271 a0001c0004t0027g0276 |
3 | NA18946.hp2 NA18963.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1175-2658C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6115330 | |||||||
chr17:6115367 | G | A | 37 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0001g0096 others(34): Show |
37 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1175-2621G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6115367 | |||||||
chr17:6115457 | A | T | 407 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(404): Show |
423 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(420): Show |
intron_variant | MODIFIER | c.1175-2531A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6115457 | |||||||
chr17:6115473 | G | C | 2 | a0001c0002t0014g0171 a0001c0002t0062g0173 |
2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1175-2515G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6115473 | |||||||
chr17:6115498 | T | C | 3 | a0001c0003t0014g0256 a0001c0003t0031g0206 a0001c0003t0035g0245 |
3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1175-2490T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6115498 | |||||||
chr17:6115514 | CA | C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0102 others(46): Show |
52 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1175-2469delA | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | 6115514 | ||||||
chr17:6115592 | C | A | 1 | a0001c0016t0003g0230 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1175-2396C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6115592 | |||||||
chr17:6115633 | C | T | 5 | a0001c0001t0002g0071 a0001c0001t0002g0076 a0001c0001t0002g0078 others(2): Show |
5 | NA18955.hp1 NA18969.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.1175-2355C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6115633 | |||||||
chr17:6115719 | C | T | 3 | a0001c0004t0003g0308 a0001c0004t0011g0271 a0001c0004t0027g0276 |
3 | NA18946.hp2 NA18963.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1175-2269C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6115719 | |||||||
chr17:6115720 | G | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0102 others(38): Show |
44 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1175-2268G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6115720 | |||||||
chr17:6115780 | GACAGGGA others(5): Show |
G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0087 others(31): Show |
35 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1175-2205_1175-219 others(16): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | 6115780 | ||||||
chr17:6115894 | C | A | 3 | a0001c0004t0002g0011 a0001c0004t0002g0288 a0001c0004t0068g0011 |
3 | HG00544.hp1 NA19011.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1175-2094C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6115894 | |||||||
chr17:6116135 | T | C | 1 | a0001c0004t0002g0288 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1175-1853T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6116135 | |||||||
chr17:6116314 | A | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0087 others(42): Show |
46 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1175-1674A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6116314 | |||||||
chr17:6116353 | C | T | 25 | a0001c0001t0001g0161 a0001c0001t0008g0259 a0001c0002t0001g0388 others(22): Show |
25 | HG00544.hp1 HG00621.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1175-1635C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6116353 | |||||||
chr17:6116400 | T | TCA | 23 | a0001c0001t0001g0144 a0001c0001t0001g0370 a0001c0001t0002g0268 others(20): Show |
23 | HG00408.hp1 HG01167.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1175-1568_1175-156 others(6): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | 6116400 | ||||||
chr17:6116400 | TCA | T | 81 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0052 others(78): Show |
84 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1175-1568_1175-156 others(6): Show |
WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | 6116400 | ||||||
chr17:6116454 | C | T | 2 | a0004c0010t0040g0042 a0004c0010t0040g0043 |
2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1175-1534C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6116454 | |||||||
chr17:6116960 | C | A | 1 | a0001c0001t0002g0298 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1175-1028C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6116960 | |||||||
chr17:6117109 | A | C | 1 | a0001c0001t0002g0103 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1175-879A>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6117109 | |||||||
chr17:6117141 | G | A | 341 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(338): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1175-847G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6117141 | |||||||
chr17:6117157 | C | T | 9 | a0001c0002t0001g0227 a0002c0006t0002g0028 a0002c0006t0005g0159 others(6): Show |
9 | HG01070.hp1 HG01109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1175-831C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6117157 | |||||||
chr17:6117252 | C | G | 5 | a0001c0001t0007g0320 a0001c0002t0015g0036 a0001c0002t0023g0188 others(2): Show |
5 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1175-736C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6117252 | |||||||
chr17:6117361 | T | C | 5 | a0001c0002t0004g0041 a0001c0002t0020g0192 a0001c0002t0026g0200 others(2): Show |
5 | HG02258.hp1 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1175-627T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6117361 | |||||||
chr17:6117478 | G | C | 1 | a0001c0001t0001g0261 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1175-510G>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6117478 | |||||||
chr17:6117679 | G | A | 36 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0001g0096 others(33): Show |
36 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1175-309G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 7/8 | chr17 | 6117679 | |||||||
chr17:6118221 | C | T | 252 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(249): Show |
264 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1375+33C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6118221 | |||||||
chr17:6118254 | C | T | 1 | a0001c0001t0005g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1375+66C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6118254 | |||||||
chr17:6118351 | G | T | 2 | a0001c0002t0085g0284 a0008c0012t0086g0283 |
2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1375+163G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6118351 | |||||||
chr17:6118386 | C | A | 2 | a0001c0001t0001g0005 a0001c0001t0005g0220 |
3 | HG01255.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1375+198C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6118386 | |||||||
chr17:6118551 | G | A | 1 | a0001c0001t0001g0393 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1375+363G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6118551 | |||||||
chr17:6118575 | C | T | 12 | a0001c0001t0004g0341 a0001c0001t0035g0035 a0001c0001t0048g0349 others(9): Show |
12 | HG01070.hp1 HG01109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1375+387C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6118575 | |||||||
chr17:6118607 | A | T | 1 | a0001c0002t0004g0377 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1375+419A>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6118607 | |||||||
chr17:6118694 | T | G | 3 | a0001c0001t0001g0024 a0001c0001t0019g0150 a0001c0001t0019g0304 |
3 | NA18962.hp1 NA18977.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1375+506T>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6118694 | |||||||
chr17:6118819 | C | G | 1 | a0001c0004t0001g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1375+631C>G | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6118819 | |||||||
chr17:6118870 | C | T | 9 | a0001c0001t0007g0320 a0001c0002t0014g0171 a0001c0002t0015g0036 others(6): Show |
9 | HG02280.hp2 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1375+682C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6118870 | |||||||
chr17:6119094 | G | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(234): Show |
246 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.1375+906G>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119094 | |||||||
chr17:6119106 | T | C | 1 | a0001c0003t0004g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1375+918T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119106 | |||||||
chr17:6119138 | C | A | 12 | a0001c0001t0004g0341 a0001c0001t0035g0035 a0001c0001t0048g0349 others(9): Show |
12 | HG01070.hp1 HG01109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1375+950C>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119138 | |||||||
chr17:6119410 | G | A | 1 | a0001c0002t0005g0139 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1376-899G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119410 | |||||||
chr17:6119476 | G | A | 35 | a0001c0001t0001g0261 a0001c0001t0001g0329 a0001c0001t0002g0303 others(32): Show |
37 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1376-833G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119476 | |||||||
chr17:6119566 | C | T | 1 | a0002c0007t0003g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1376-743C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119566 | |||||||
chr17:6119641 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
272 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1376-668C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119641 | |||||||
chr17:6119647 | C | T | 1 | a0001c0002t0049g0366 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1376-662C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119647 | |||||||
chr17:6119648 | T | C | 11 | a0001c0002t0017g0015 a0001c0002t0017g0163 a0001c0002t0022g0047 others(8): Show |
11 | HG01070.hp1 HG01109.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1376-661T>C | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119648 | |||||||
chr17:6119664 | C | T | 1 | a0001c0003t0004g0189 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1376-645C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119664 | |||||||
chr17:6119785 | G | A | 1 | a0002c0006t0002g0028 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1376-524G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119785 | |||||||
chr17:6119787 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1376-522C>T | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119787 | |||||||
chr17:6119835 | G | A | 2 | a0001c0002t0004g0191 a0001c0002t0081g0376 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1376-474G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119835 | |||||||
chr17:6119944 | G | A | 1 | a0001c0001t0002g0331 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1376-365G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6119944 | |||||||
chr17:6120018 | G | A | 337 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(334): Show |
352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.1376-291G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6120018 | |||||||
chr17:6120136 | G | A | 74 | a0001c0001t0001g0081 a0001c0001t0001g0094 a0001c0001t0001g0161 others(71): Show |
74 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.1376-173G>A | WSCD1 | ENSG00000179314.16 | transcript | ENST00000317744.10 | protein_coding | 8/8 | chr17 | 6120136 |